Authorized Sources of Narcotic Raw Materials, 6843-6851 [E8-2142]
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Federal Register / Vol. 73, No. 25 / Wednesday, February 6, 2008 / Rules and Regulations
sentence add the word ‘‘test’’ before the
word ‘‘frame’’.
I d. Redesignate paragraphs (a)(6)(v)
through (a)(6)(ix) as paragraphs (a)(6)(vi)
through (a)(6)(x) respectively;
redesignate the fourth through the last
sentence of paragraph (a)6)(iv) as
paragraph (a)(6)(v); and add the heading
‘‘Burner inlet lines.’’ to newly
designated paragraph (a)(6)(v).
I e. In redesignated paragraph (a)(6)(vi)
before the word ‘‘Frame’’ in the heading
of the paragraph add the word
‘‘Burner’’.
I f. In redesignated paragraph (a)(6)(vii)
in footnote 1 remove the phrase ‘‘3 inch
ID by inch OD’’ and add in its place the
phrase ‘‘0.25 inch ID by 0.4 inch OD’’.
I g. In redesignated paragraph (a)(6)(ix),
second sentence, remove the number
‘‘70’’ and in its place add ‘‘140 ± 5’’;
after the number ‘‘20’’ add ‘‘± 1’’; after
the word ‘‘Figure’’ remove the number
‘‘8’’ and add the number ‘‘7’’ in its
place.
I h. In paragraph (b)(1)(ii), the last
sentence, remove ‘‘20 ± .5’’ and in its
place add ‘‘20 ± 1’’.
I i. In paragraph (d)(1), first sentence,
before ‘‘0.5 m/s’’ add the words ‘‘no
more than’’.
I j. In paragraph (d)(2), third sentence,
remove the word ‘‘bed’’ and add in its
place the word ‘‘test’’; remove the fourth
sentence and add in its place ‘‘Carefully
center the foundation on top of the test
frame to eliminate any gaps between the
bottom periphery of the foundation and
the inside edges of the test frame. If the
mattress is to be tested alone, place it
similarly. A mattress tested with its
foundation should be centered
longitudinally and laterally on the
foundation.’’.
I k. In paragraph (e) remove the number
‘‘(ix)’’ and add in its place the number
‘‘(x)’’.
I l. In paragraph (f) move the third
sentence so that it becomes the first
sentence of the paragraph.
I m. In paragraph (h)(1)(iv) add at the
end of the first sentence the words ‘‘or
another dimension that meets the
requirements for a specific sample’’;
remove the last sentence of the
paragraph.
I n. In paragraph (h)(2)(i) remove the
last sentence and add it in its place the
words ‘‘Use a sufficient length of duct
tape (platen to mattress top) to assure
that the platen stays firmly against the
surfaces of the mattress.’’.
I o. In paragraph (h)(2)(iv) remove the
first sentence and add in its place the
sentence ‘‘Make the horizontal burner
parallel to the top of the platen (within
3 mm (1⁄8 inch) over the burner tube
length); when properly parallel, it
should not be possible to insert the 3
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mm flat stock under either burner end
by bending the copper tube section
appropriately.’’.
I p. In paragraph (h)(2)(viii), first
sentence, remove the word ‘‘its’’ and
add in its place the words ‘‘the vertical
burner’’; move the reference to footnote
9 to the end of the second to last
sentence in the paragraph.
I q. In paragraph (i)(2)(i) in the second
to last sentence remove the abbreviation
‘‘ca.’’ and add in its place the word
‘‘approximately’’.
I 3. Section 1633.12 is amended as
follows:
I a. In paragraph (a)(6)(iii) before ‘‘;
and’’ add the sentence ‘‘Such
foundation(s) shall be clearly identified
by a simple and distinct name and/or
number on the mattress label’’.
I b. In paragraph (d) after the word
‘‘paragraphs’’ remove the phrase
‘‘(a)(7)(i) and (a)(7)(ii), and (a)(7)(iii)’’
and add in their place the phrase
‘‘(a)(6)(i) through (iii) and (a)(7)(i)
through (iii)’’.
Dated: January 30, 2008.
Todd Stevenson,
Secretary, Consumer Product Safety
Commission.
[FR Doc. E8–2027 Filed 2–5–08; 8:45 am]
BILLING CODE 6355–01–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
21 CFR Part 1312
[Docket No. DEA–282F]
RIN 1117–AB03
Authorized Sources of Narcotic Raw
Materials
Drug Enforcement
Administration (DEA), Department of
Justice.
ACTION: Final rule.
AGENCY:
SUMMARY: The Drug Enforcement
Administration (DEA) is amending the
list of non-traditional countries
authorized to export narcotic raw
materials (NRM) to the United States by
removing Yugoslavia and adding Spain.
This rule provides DEA registered
importers with another potential source
from which to purchase NRM that are
used in the production of controlled
substances for medical purposes in the
United States.
DATES: Effective Date: This rule is
effective March 7, 2008.
FOR FURTHER INFORMATION CONTACT:
Christine A. Sannerud, PhD, Chief, Drug
and Chemical Evaluation Section, Office
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of Diversion Control, Drug Enforcement
Administration, Washington, DC 20537,
telephone (202) 307–7183.
SUPPLEMENTARY INFORMATION:
Background and Legal Authority
DEA enforces the Comprehensive
Drug Abuse Prevention and Control Act
of 1970, often referred to as the
Controlled Substances Act (CSA) and
the Controlled Substances Import and
Export Act (21 U.S.C. 801, et seq.), as
amended. DEA regulations
implementing these statutes are
published in Title 21 of the Code of
Federal Regulations (CFR), Parts 1300 to
1316. These regulations are designed to
ensure that there is a sufficient supply
of controlled substances for legitimate
medical, scientific, research, and
industrial purposes and to deter the
diversion of controlled substances to
illegal purposes. The CSA and its
implementing regulations are consistent
with United States treaty obligations
that, among other things, address the
production, import, and export of
controlled substances.
Controlled Substances
Controlled substances are drugs that
have a potential for abuse and
psychological and physical dependence,
including opiates, stimulants,
depressants, hallucinogens, anabolic
steroids, and drugs that are immediate
precursors of these classes of
substances. DEA lists controlled
substances in 21 CFR Part 1308. The
substances are divided into five
schedules. Schedule I substances have a
high potential for abuse and have no
accepted medical use in treatment in the
United States. These substances may
only be used for research, chemical
analysis, or manufacture of other drugs.
Substances listed in schedules II—V
have accepted medical uses but also
have potential for abuse and
psychological and physical dependence.
Narcotic raw materials (opium, poppy
straw, and concentrate of poppy straw
(CPS)) are in schedule II and are the
materials from which morphine,
codeine, thebaine and oripavine are
extracted for purposes of manufacturing
a number of schedule II and III
controlled substances.
Sources of Narcotic Raw Materials
In May 1979, the United Nations’
Economic and Social Council (ECOSOC)
adopted Resolution 471, which called
on importing countries such as the
United States to support traditional
suppliers of NRM and to limit imports
from non-traditional supplying
countries. The resolution, which was
reaffirmed by ECOSOC in 1981, was
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adopted to limit overproduction of
NRM, to restore a balance between
supply and demand, and to prevent
diversion to illicit channels. The United
States, based on long-standing policy,
does not cultivate or produce NRM, but
relies solely on opium, poppy straw,
and CPS produced in other countries for
the NRM necessary to meet the
legitimate medical needs of the United
States. In response to Resolution 471, on
August 18, 1981, DEA published a final
rule specifying certain source countries
of NRM (46 FR 41775); the rule is
frequently referred to as the 80/20 rule.
Under the final rule, currently codified
at 21 CFR 1312.13(f) and (g), NRM can
be imported from only seven countries.
Traditional suppliers India and Turkey
must be the source of at least 80 percent
of the United States’ requirement for
NRM. Five non-traditional supplier
countries—France, Poland, Hungary,
Australia, and Yugoslavia—may be the
source of not more than 20 percent. The
80/20 rule is calculated based on the
amount of morphine alkaloid contained
in the NRM. The United States
continues to reaffirm its support of the
original resolution by supporting similar
resolutions each year at the Commission
on Narcotic Drugs.
Just as with DEA’s 1979 Federal
Register publication first proposing the
80/20 rule (44 FR 33695), it is important
to recite here some of the central
principles of Resolution 471, which
remain crucial today:
Noting that in recent years there has been
considerable stepping up of morphine
producing capacity for export, leading to a
situation of substantial overproduction of
opiates,
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Recognizing that it is essential to bring
about a proper balance between the global
supply and demand,
Taking note of the continued reliance
placed by the world community on countries
constituting the traditional sources of supply
for its medical needs of opiate raw materials
and the positive response of these countries
in meeting the world requirements and their
contribution in the maintenance of effective
control systems;
Bearing in mind that the treaties which
establish this system are based on the
concept that the number of producers of
narcotic materials for export should be
limited in order to facilitate effective control;
* * *
In view of these principles underlying
Resolution 471, DEA stated in proposing
the 80/20 rule in 1979:
The United States is a significant importer
of narcotic raw materials. Its manufacturers
account for one-third of the world morphine
manufacturing capacity, most of which is
consumed within the United States in the
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form of codeine.1 The worldwide overproduction of narcotic raw materials and
[Resolution 471] make it necessary for the
United States to reevaluate past and present
narcotic policies.
Historically, the United States has relied
exclusively upon imports of opium gum to
manufacture our narcotic medical supplies
instead of cultivating opium poppies in the
United States. The rationale behind this 57year-old policy, which foregoes [sic] U.S.
self-sufficiency, was to set an example to the
world community to refrain from
overproduction and to limit the number of
opium-producing nations to a minimum.
[44 FR 33696, June 12, 1979]
The foregoing principles remain
central to United States drug control
policy and this final rule amending the
80/20 rule.
Of the countries included in the 80/
20 rule, India is the only country that
cultivates poppies for production of
opium. All other exporting countries
use the CPS method of NRM
production, a method that allows the
plant to go to seed; portions of the plant
are then processed into a concentrate. It
is generally believed that CPS is less
divertible than opium. CPS may be rich
in morphine (CPS–M), rich in thebaine
(CPS–T), or rich in oripavine (CPS–O).
The United States imports the majority
of its CPS–M from Turkey, with
Australia supplying the vast majority of
the balance. The vast majority of CPS–
T and all CPS–O are imported from
Australia.
The 80/20 rule was established based
on traditional import amounts and on
the United Nations resolution calling on
member nations to support traditional
sources that have been reliable suppliers
and to take measures that curtail
diversion. The United States allowed a
limited number of non-traditional
suppliers to have access to the United
States market based on past commercial
relationships and on the desirability of
preserving alternative sources. This
approach was consistent with the
United Nations Resolution because it
supported India and Turkey and
ensured an adequate and uninterrupted
supply of NRM while limiting the
number of supplying countries. Over the
last ten years, pursuant to the 80/20
rule, DEA registered importers of NRM
have imported 90 percent of United
States NRM requirements from
traditional suppliers India and Turkey.
DEA continues its support of the intent
of the 80/20 rule.
1 Today, the United States remains a significant
importer of narcotic raw material. Its manufacturers
currently account for one-fourth of the world
morphine manufacturing capacity, with roughly
two-thirds being utilized for the production of
codeine, which is consumed as either codeine or
hydrocodone.
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On June 6, 2005, the Kingdom of
Spain (hereinafter referred to as Spain)
petitioned DEA seeking to be added to
the list of non-traditional suppliers.
Spain stated four reasons that granting
its petition would be consistent with
United States interests:
• The change would be consistent
with the 80/20 rule because it maintains
India and Turkey as the two traditional
supplier countries, that is, Spain does
not seek to be added to the list of
traditional suppliers.
• The change would ensure adequate
supplies of NRM.
• The change would not result in
diversion because Spain maintains strict
control and oversight over the
cultivation and distribution of NRM.
• The change would allow DEA to
monitor diversion and maintain costeffective supplies.
In its petition, Spain explained that in
the early 1970s, Spanish pharmaceutical
firms sought authorization to cultivate
opium poppies to produce NRM. In
1973, the Government of Spain
authorized a single firm, Alcaliber, S.A.,
to cultivate, harvest, store, and prepare
extracts from the opium poppy. Spain is
now the fifth largest cultivator of opium
poppies; Spain is the fourth largest
producer of CPS and the third largest
exporter of CPS–M.2 Spain has ratified
international agreements to control
production and commerce in opium
products. As stated in its petition, Spain
has implemented a comprehensive
regulatory regime for controlling the
cultivation, production, and export of
NRM in accordance with international
treaty requirements. The petition stated
that this control ensures that NRM
produced in Spain are not diverted to
illicit uses.
After review of the petition, DEA
published a Notice of Proposed
Rulemaking (NPRM) in the Federal
Register on October 4, 2006 (71 FR
58569) to amend the list of nontraditional countries authorized to
export NRM to the United States.
Specifically, the proposed rule sought to
revise the list of non-traditional
suppliers by removing Yugoslavia and
replacing it with Spain. At that time,
DEA had determined that the successor
states to Yugoslavia no longer produced
NRM for export beyond Yugoslavia’s
prior border (e.g., Serbia and
Montenegro reported exports to the
Republic of Macedonia (hereinafter
referred to as Macedonia) only).
Therefore, DEA concluded that
2 ‘‘Narcotic Drugs: Estimated World Requirements
for 2005—Statistics for 2003’’, Tables II and XIII;
International Narcotics Control Board (E/INCB/
2004/2).
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replacing Yugoslavia with Spain would
continue to limit the number of nontraditional suppliers to the United
States while ensuring the availability of
an adequate number of sources of NRM
for United States manufacturers. The
proposed change would not otherwise
affect the implementation of the 80/20
rule.
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Comments Received
Following publication of the Notice of
Proposed Rulemaking on October 4,
2006, DEA received a request for a 60day extension to the comment period.
On December 1, 2006, DEA extended
the comment period of the proposed
rule to January 3, 2007 (71 FR 69504).
During the comment period, DEA
received 14 comments from 13
interested parties. Five comments were
received from the following countries:
Australia, Spain, Macedonia, and
Turkey. One of the comments received
from a foreign Government was a joint
comment with a foreign control board.
Three comments were received from
three DEA-registered importers of NRM;
one comment was received from a DEAregistered opiate manufacturer; one
comment was received from a non-DEA
registered firm; two comments were
received from two foreign NRM
manufacturers; and two comments were
received from one individual. As part of
the above-listed comments, DEA also
received a request to extend the
comment period, and four requests for
a hearing.
After the comment period had ended,
DEA received an additional comment
from a foreign NRM manufacturer. This
prompted two additional late
comments, one from the foreign control
board which previously commented on
the NPRM and the other from the
foreign government associated with that
foreign control board. Specifically, both
commenters sought clarification from
DEA on the status of the late comment,
which DEA had administratively added
to the docket. The Administrative
Procedure Act (APA) does not address
the issue of late comments, and the
United States courts generally defer to
federal agencies in their handling of late
comments. It is the policy of the DEA
that comments not properly filed, e.g.,
comments postmarked after the close of
a comment period, will not be
considered by the agency in its
deliberative process. Accordingly, the
late comment from the foreign NRM
manufacturer was not considered by
DEA in this Final Rule. All comments
received during the comment period are
summarized here and discussed further
below.
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Comments in Support of DEA’s NPRM
Four of the commenters supported the
proposed rule. These commenters
included the Government of Spain, a
DEA registered NRM importer, one
foreign NRM manufacturer, and a DEAregistered opiate manufacturer. One of
the DEA registrants commented that the
need to ensure an adequate number of
sources of NRM for DEA-registered
NRM importers is ‘‘most keenly felt in
CPS–T and CPS–O, for which the U.S.
demand is rapidly growing and in
which global supply sources to the U.S.
are currently quite limited.’’
Comments Raising Concerns to DEA’s
NPRM
Nine of the commenters raised
various concerns regarding the NPRM.
These commenters included the
Government of Australia, the
Government of Macedonia, and the
Government of Turkey; a foreign NRM
control board; two DEA-registered
importers of NRM; one non-DEAregistered firm; one foreign NRM
manufacturer; and one individual.
Four commenters claimed that the
proposed rule would exacerbate current
global oversupplies of NRM and
therefore disrupt the balance between
the supply of and demand for NRM.
Three commenters claimed that the
proposed rule was not consistent with
the intent of the 80/20 rule or
international resolutions. Three
commenters claimed that the proposed
rule was not necessary to assist the
United States in maintaining cost
effective supplies of NRM. Three
commenters questioned DEA’s decision
to replace Yugoslavia with Spain.
The following additional concerns
were raised. One commenter believed
that the addition of Spain to the list of
non-traditional NRM producing
countries would lead to a proliferation
of NRM-producing countries. The
commenter, however, did not provide
further information as to how this
rulemaking would specifically lead to a
proliferation of NRM-producing
countries. Additionally, one commenter
claimed that Spain has diversion
occurring within its borders and that it
could not be proven that the addition of
Spain to the list of non-traditional
countries would not lead to an increase
in diversion within Spain. While the
commenter provided a general
statement regarding the diversion of
controlled substances, the commenter
did not provide any specific evidence
regarding the diversion of narcotic raw
material specifically cultivated for
lawful purposes in Spain. Due to the
lack of substantiation for the claims
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discussed above, these comments are
not addressed further in this
rulemaking.
Request for Hearing
Four commenters requested that DEA
hold an administrative hearing in this
matter. Two of these commenters
requested a hearing prior to the issuance
of the final rule. One of these
commenters stated that a hearing was
appropriate ‘‘given the gravity and
complexity of the issues involved.’’ The
other commenter stated that a hearing
would ‘‘provide interested parties with
the fullest opportunity to make their
views known and have their positions
considered.’’ These commenters did not
proffer any specific information beyond
that submitted in the written comments,
however, that would be brought to light
if their requests for a hearing were
granted. DEA has determined that an
oral hearing prior to the issuance of this
rule is unnecessary. The amendment of
the 80/20 rule to substitute one nontraditional country for another that no
longer exists in the form it did at the
time of the promulgation of the original
rule does not represent a major change
in DEA policy or procedure. Moreover,
DEA has carefully considered all of the
comments received in connection with
the proposal, and finds that the
comments fully set forth the issues
relevant to this rulemaking. Based on
information provided in the comments,
information provided in technical
reports by the International Narcotics
Control Board (INCB), and information
provided by U.S. importers of NRM
pursuant to DEA regulations, DEA has
been able fully to address the relevant
issues set forth in the comments and has
determined that conducting a hearing
would not materially add to the
administrative record. DEA has
concluded, therefore, that such a
hearing would be unnecessary.
Two other commenters requested a
hearing following the issuance of the
final rule, if it is issued. Such a request
does not conform procedurally with
traditional rulemaking procedures
under the APA, under which—if an
agency holds a hearing in connection
with a proposed rule—it is held prior to
the issuance of the final rule. Moreover,
neither the CSA nor DEA regulations
provide for an administrative hearing to
‘‘appeal’’ the promulgation of a final
rule. Pursuant to 21 U.S.C. 877,
exclusive jurisdiction for appeals of
DEA final decisions such as this rule
rests with the United States Courts of
Appeals. Accordingly, the requests for a
hearing if the final rule is issued are
denied.
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Other Comments Received
One of the commenters wrote that if
the proposal sought to change the
method by which the 80/20 rule was
calculated, then the commenter would
object to the proposed rule. As noted
previously, the 80/20 rule is calculated
based on the amount of morphine
alkaloid contained in the NRM. Since
DEA’s proposed rule and this
rulemaking do not affect how the 80/20
rule is calculated, this matter is not
addressed further in this rulemaking.
One commenter submitted two
comments. One of these comments
stated, ‘‘So we are deciding who to
allow to do the exporting of substances
that are used to make heroin? We allow
this? And then kick down the doors of
terminally ill patients who smoke
marijuana just to ease their
pain. * * *’’ The other comment
promoted the use of hallucinogens.
NRM imported into the United States
pursuant to this rule are used to make
legitimate medicines that are used to
treat pain, not to manufacture heroin.
Heroin production and the use of
marijuana and hallucinogens are not the
subject of this rulemaking; these matters
are therefore not addressed further in
this rulemaking.
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Support for DEA’s NPRM
Adequate Supply of NRM
Three commenters addressed the need
to ensure adequate supplies of NRM for
United States markets. One commenter
noted that the need to ensure an
adequate number of sources of NRM for
DEA registered NRM importers was
‘‘most keenly felt in CPS–T and CPS–O,
for which the U.S. demand is rapidly
growing and in which global supply
sources to the U.S. are currently quite
limited.’’
DEA Response: DEA agrees that
United States sources of NRM are
limited based on data it collects
quarterly from DEA registered importers
pursuant to 21 CFR 1304.31. The data
collected in these reports include the
relative amounts of morphine, codeine,
thebaine and oripavine contained in
each individual NRM import to the
United States as reported by each of the
five DEA registered NRM importers. In
response to this comment, DEA
conducted an analysis of the source of
each of the primary alkaloids available
in current NRM: morphine, thebaine
and oripavine. DEA notes that, in 2006,
imports of NRM had as their source,
four of the seven countries authorized to
export NRM to the United States,
specifically India, Turkey, Australia and
France. United States importers have
not imported NRM from Poland or
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Yugoslavia since at least 1985, and
imports from Hungary were minimal in
the mid to late 1990s and have ceased
altogether since 2002. No imports from
Poland, Yugoslavia, or Hungary are
anticipated in 2007. Since NRM contain
a mixture of these alkaloids, DEA’s
review of the NRM import situation
(below) is expressed in terms of the
amount of morphine, thebaine, and
oripavine contained in imported NRM.
Morphine: Morphine is the principal
alkaloid in Indian opium and Turkish
CPS–M and has historically been the
principal alkaloid extracted from NRM
in the United States. Morphine
continues to be utilized in the United
States for the manufacture of morphinebased pharmaceutical products; the
manufacture of codeine, which is
utilized to manufacture codeine-based
pharmaceutical preparations and
hydrocodone; and the manufacture of
hydromorphone. Based on an analysis
of information received for 2006,
imports of NRM totaled 124,000 kg of
morphine (124.0 metric tons (MT)),
having the following countries as its
source: Turkey (59.9 MT morphine; 48.3
percent), India (43.9 MT morphine; 35.4
percent), and Australia (20.4 MT
morphine; 16.5 percent).3 When
reviewing imports of morphine over the
last 10 years (1997–2006), United States
importers obtained commercial
quantities of morphine from India,
Turkey, and Australia, with lesser
amounts obtained from France and
Hungary. DEA concludes as a result that
the United States has at least three
geographically distinct countries from
which morphine is obtained, each with
large production capacity on which the
United States could rely if any of those
countries were to experience a hardship
(i.e., crop failure, labor strife, etc.).
Adding Spain would provide DEA
registered importers with a fourth
country from which to purchase NRM.
Thebaine: Thebaine is the principal
alkaloid in CPS–T. CPS–T is available to
the United States market from Australia
and France. Thebaine is also present in
Indian opium at approximately one
sixth the level of morphine, thus the
amount of thebaine obtained from India
is directly related to the amount of
morphine that United States importers
import from India. In the United States,
thebaine is utilized for the manufacture
of oxycodone, a schedule II controlled
substance. More recently, oxycodone
has been utilized for the manufacture of
oxymorphone, another schedule II
controlled substance.
3 Percentages may not add to 100 percent due to
rounding.
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Oxycodone use in the United States
has increased tremendously over the
last 10 years. For example, the aggregate
production quota for oxycodone, which
represents the maximum amount that
may be manufactured in the United
States to meet the estimated medical,
industrial, scientific, and research needs
of the United States; for lawful export
requirements; and the maintenance of
reserve stocks, has increased over the
last decade from 5,275 kg in 1997 to
49,200 kg in 2006. The large increase in
oxycodone use in the United States
followed the approval and marketing in
1995 of a high dose, single-entity,
extended-release drug formulation
known as OxyContin. Although DEA
remains concerned over the diversion
and abuse of OxyContin and other
formulations that contain high doses of
potent schedule II controlled
substances, the Food and Drug
Administration continues to advise DEA
of double-digit growth in the oxycodone
market through 2008. This provides
evidence that the demand for thebainerich NRM that must be imported into
the United States for this purpose will
also continue to increase.
When the same 2006 quarterly
statistical import data was reviewed for
thebaine, DEA noted that 78.2 MT of
thebaine was imported into the United
States in 2006, having as its source the
following countries: Australia (66.8 MT
of thebaine; 85.4 percent), India (7.1 MT
of thebaine; (9.1 percent), and France
(4.1 MT of thebaine; 5.2 percent).4 Thus,
Australia was the source of 85 percent
of United States thebaine requirements
in 2006.5 For comparison, in 2005, 73
percent of the 65.4 MT of thebaine
imported into the United States had
Australia as it source, and, in 2004, 75
percent of the 66.8 MT were imported
from Australia. In 2007, United States
importers have reported their plans to
import 92 percent of their thebaine
requirements from Australia; they
planned to import the remaining 8
percent solely from India.
DEA notes that Australia has a stellar
record in providing thebaine-rich NRM
to the United States, with little (if any)
record of diversion. DEA further notes
that the United States and Australia
have excellent relations in this area, and
contrary to comments made by some
commenters to this NPRM, DEA’s
proposed rule and this final rule in no
4 Ibid.
5 As discussed previously, The 80/20 rule is
calculated based on the amount of morphine
alkaloid contained in the NRM. As this discussion
relates to the amount of thebaine alkaloid in the
NRM, not morphine, the 85 percent obtained by the
United States from Australia does not violate
principles of the 80/20 rule.
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Federal Register / Vol. 73, No. 25 / Wednesday, February 6, 2008 / Rules and Regulations
way suggest that Australia has ‘‘not
ensured an adequate and uninterrupted
supply’’ of NRM to the United States.
DEA remains mindful, however, of the
potential impact of a hardship (i.e., crop
failure, labor strife, etc.) in Australia
that could lead to a temporary lack of
availability of thebaine to the United
States market. In this circumstance, the
United States would be required to
obtain much larger volumes of NRM
from either India or France in order to
meet thebaine demand. Although
France has demonstrated the capability
of exporting up to 16 MT of thebaine in
a single year to the United States,
India’s capacity to export thebaine, as
mentioned above, is directly related to
the amount of morphine that importers
wish to import from India consistent
with the 80/20 rule. Therefore,
importing vast quantities of Indian
opium to meet United States thebaine
demands would be impractical because
it would result in the importation into
the United States of excessive amounts
of morphine, which could then be the
subject of diversion and abuse. Thus,
the amount of thebaine that could be
derived from India, consistent with
United States requirements for
morphine contained in Indian opium, is
likely to be 6–8 MT annually. DEA
concludes that the United States has
limited sources from which to obtain
thebaine derived from NRM. The United
States relies on three countries for
thebaine, but two of these countries
have a limited capacity to support the
increasing size of the United States’
market for thebaine. DEA notes that, in
2004, the Government of Spain reported
for the first time commercial production
of CPS–T, so Spain would represent a
fourth country from which CPS–T could
be imported. As a result, this rule will
provide DEA registered importers with
another source from which to purchase
CPS–T for the production of medicines.
Oripavine: Oripavine, a schedule II
controlled substance, is the principal
alkaloid found in Australian CPS–O and
is a minor constituent in French CPS–
T. Oripavine is becoming an
increasingly important intermediate in
the United States for the manufacture of
buprenorphine, a schedule III controlled
substance, oxymorphone, and a number
of controlled and non-controlled
substances referred to generally as
‘‘opiate antagonists’’ (naltrexone for
example, and its derivatives). Using the
same import data, DEA notes that, in
2006, 9.7 MT of oripavine was imported
into the United States having Australia
as its source, virtually 100 percent of the
United States’ oripavine requirements.
In 2005, 4.1 MT were imported from
Australia and in 2004, 9.4 MT were
imported with roughly 86 percent
imported from Australia. United States
importers have reported their plans to
import 100 percent of the 9.7 MT of
oripavine from Australia in 2007. DEA
therefore concludes that the United
States has limited sources from which to
obtain oripavine derived from NRM.
Objections to DEA’s NPRM
Global Oversupply of Narcotic Raw
Materials
The Government of Australia’s
primary concern regarding DEA’s
proposed rule is that this rule would
‘‘exacerbate global oversupply’’ of NRM.
In its comment, the Government of
Australia pointed to statistical data
published by the INCB in its report,
‘‘Narcotic Drugs: Estimated World
Requirements for 2006—Statistics for
2004,’’ which the Government of
Australia characterized as
demonstrating that global production of
both morphine-rich and thebaine-rich
NRM have been in excess of global
utilization since at least 2001. As a
result of overproduction, the
Government of Australia argued, global
supplies have increased.
The DEA-registered NRM importer
stated that ‘‘Alcaliber [the sole Spanish
poppy cultivator] made a significant
investment in capacity, dramatically
increased production contributing
significantly to global overproduction
and excess stocks, and now wants
access to the U.S. market to allow it to
increase production further to help
recover its investment.’’ The importer
further stated that the Notice of
Proposed Rulemaking sent the message
6847
that ‘‘If a country adds production
capacity, uses it aggressively and
thereby contributes to the world’s build
up of excess stocks, the U.S. will
accommodate this behavior and reward
it with access to the U.S. market. The
U.S. will simply delete a smaller
producer from the list.’’ This commenter
also stated that ‘‘Spain was arguably the
primary source of this build up in
excess morphine stocks.’’
Finally, the foreign opiate
manufacturer stated that ‘‘Spain’s rapid
expansion of its domestic industry, its
aggressive approach to building export
markets, its building of clearly excessive
stockpiles and capacity, and supply into
a market already in over-supply is not
* * * broadly in accordance with the
obligations under the Single
Convention, or the Resolutions.’’
DEA Response: DEA disagrees that
Spain is the ‘‘primary’’ source of any
build-up of global excesses in morphine
stocks. Instead, DEA concludes that all
countries that produce NRM contribute
to the current global excess of NRM.
Among many of the requirements of
NRM-producing countries, in
accordance with the Single Convention
on Narcotic Drugs, 1961, is a
requirement to provide annual statistics
to the INCB, including estimated
amounts of NRM to be cultivated and
the amount of NRM to be produced
therefrom. The INCB utilizes these
estimates along with other statistical
data it collects, in accordance with the
Single Convention, to monitor and
analyze the global supply of and
demand for NRM. The results of this
analysis are published in a technical
report series, which in 2004 was
entitled, ‘‘Narcotic Drugs: Estimated
World Requirements for 2006; Statistics
for 2003.’’ The analysis conducted by
the INCB and the statistical reports
published continue to be an excellent
resource for governments of consumer
countries such as the United States. A
review of this report series for 2004 and
2005 was conducted with relevant
statistical data provided in Tables 1 and
2.
Analysis for Morphine-Rich Poppies
TABLE 1.—‘‘GLOBAL CULTIVATION OF MORPHINE-RICH POPPIES (HECTARES) FOR LICIT PURPOSES OTHER THAN
PRODUCTION OF OPIUM’’
2003
(ha)
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Country
Australia ...........................................................................................................................
People’s Republic of China .............................................................................................
Czech Republic ................................................................................................................
France ..............................................................................................................................
Hungary ...........................................................................................................................
Slovakia ...........................................................................................................................
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PO 00000
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Fmt 4700
Sfmt 4700
9,811
1,250
21,045
7,919
2,937
332
E:\FR\FM\06FER1.SGM
2004
(ha)
6,644
1,000
16,030
8,312
7,084
326
06FER1
2005
(ha-est.)
6,700
1,300
25,000
8,500
14,000
550
2006
(ha-est.)
4,900
1,200
38,000
9,100
12,000
....................
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Federal Register / Vol. 73, No. 25 / Wednesday, February 6, 2008 / Rules and Regulations
TABLE 1.—‘‘GLOBAL CULTIVATION OF MORPHINE-RICH POPPIES (HECTARES) FOR LICIT PURPOSES OTHER THAN
PRODUCTION OF OPIUM’’—Continued
2003
(ha)
Country
2004
(ha)
2005
(ha-est.)
2006
(ha-est.)
Spain ................................................................................................................................
Republic of Macedonia ....................................................................................................
Turkey ..............................................................................................................................
United Kingdom ...............................................................................................................
5,732
51
99,430
1,534
5,986
91
30,343
1,534
7,002
1,500
70,000
1,500
6,002
1,500
70,000
....................
Total ..........................................................................................................................
150,041
77,350
136,052
142,702
Neither DEA, nor any commenter,
identified a single instance in these
reports in which the INCB raised
concerns over Spain’s purported role in
the global excess of production and the
resulting oversupply of NRM presently
on hand. According to this publication,
Spain was one of eleven countries that
cultivated morphine-rich poppies in
2003 for licit pharmaceutical purposes
(i.e. non-culinary use). Spain planted
5,732 hectares of poppies and produced
under cultivation and had plans to
decrease its area under cultivation in
2006 to 4.2 percent.
Although Spain remains one of the
five largest cultivators of morphine-rich
poppies in the world, DEA concludes
that Spain, like all other producer and
consumer countries, contributes to what
the INCB qualifies as a ‘‘high’’ level of
stocks of raw materials rich in
morphine.
roughly 4.7 percent of the world’s
morphine-rich poppy straw. Spain’s
share of world production of poppy
straw increased in 2004 to 10.7 percent;
the increase was attributed to both an
increase in 2004 acreage sown in Spain
and a large decrease in acreage sown by
the primary cultivator of poppies for
this purpose, Turkey. Estimates for the
‘‘area to be cultivated’’ for 2005 and
2006 suggest that Spain will be
responsible for 5.1 percent of the area
Analysis of Thebaine-Rich Poppies
TABLE 2.—‘‘GLOBAL CULTIVATION OF THEBAINE-RICH POPPIES (HECTARES) FOR LICIT PURPOSES OTHER THAN
PRODUCTION OF OPIUM’’
Country
2003
(ha)
Australia ...........................................................................................................................
People’s Republic of China .............................................................................................
France ..............................................................................................................................
Spain ................................................................................................................................
7,637
34
1,499
....................
Total ..........................................................................................................................
9,170
Australia is the principal cultivator of
thebaine-rich poppies and is responsible
for the vast majority of thebaine-rich
CPS that is produced and imported into
the United States. Although the INCB
notes that production of thebaine-rich
NRM exceeded demand substantially
until 2002, DEA notes that the primary
cultivators, Australia and France, began
decreasing areas under cultivation in
2003 and have made significant
decreases since that time in order to
bring production in line with
utilization. Although Spain noted
cultivation of thebaine-rich poppies for
the first time in 2004, it is not
responsible for excess production that
resulted in excess supplies before then.
yshivers on PROD1PC62 with RULES
Consistency With the 80/20 Rule and
International Resolutions
As stated in DEA’s Notice of Proposed
Rulemaking, the 80/20 rule was
promulgated following a resolution
adopted by the United Nations’
Economic and Social Council (ECOSOC)
in 1979. In response to the resolution in
1979, DEA published an Advance
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16:43 Feb 05, 2008
Jkt 214001
Notice of Proposed Rulemaking (44 FR
33695, June 12, 1979) and then a Notice
of Proposed Rulemaking (45 FR 9289,
February 12, 1980). The comments
resulting from the Notice of Proposed
Rulemaking led to an administrative
hearing. On August 18, 1981, DEA
published a final rule promulgating the
80/20 rule (46 FR 41775).
Objections to the current Notice of
Proposed Rulemaking pointed to
specific comments in the 1979
resolution, the Notice of Proposed
Rulemaking, the transcript of the
administrative hearing, and
considerations made by then-Acting
Administrator Francis Mullen, Jr., in
DEA’s 1981 Final Rule.
The foreign opiate manufacturer
stated that the 1979 ECOSOC resolution
called on ‘‘importing countries to * * *
take effective steps to support their
traditional supplier countries’’ and
urged ‘‘major producing and
manufacturing countries to which have
set up [sic] additional capacity in recent
years to take effective measures to
restrict substantially their production
PO 00000
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Fmt 4700
Sfmt 4700
2004
(ha)
5,578
2005
(ha-est.)
2006
(ha-est.)
1,007
996
6,500
40
1,100
500
5,300
50
1,000
1,000
7,581
8,140
7,350
levels to assure a lasting balance
between supply and demand and to
prevent drug diversion to illicit
channels.’’ The commenter believed that
‘‘[a]llowing Spain to now enter the
market directly contradicts and
undermines the objective of the Current
80/20 Rule, and rewards a country for
engaging in the very conduct the
Current 80/20 Rule, and the
Resolutions, were intended to
discourage or stop.’’
The DEA-registered NRM importer
who filed objections to the NPRM
provided a summary of the
determinations of fact made by Francis
Young, the Administrative Law Judge
(ALJ) who presided over the hearing in
1980; these findings were adopted by
then-Acting Administrator Mullen when
the final rule was promulgated. The
DEA-registered importer provided the
following summary of ALJ Young’s
determinations of fact: ‘‘(1) DEA could
lawfully promulgate the regulatory
amendments limiting the importation of
narcotic raw materials; (2) the
Administrator of DEA could lawfully
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require that a major portion of the
[NRM] imported into the United States
be produced in India and Turkey while
permitting the remainder of the U.S.
needs to be imported from other
countries which maintain adequate
control; (3) such allocation would be in
harmony with U.S. trade agreements
and would not be inconsistent with
Resolution 471 and 497; and (4) DEA
staff should determine an allocation
ratio based upon world market shares
during a recent representative period.’’
This commenter further noted that the
1981 final rule ‘‘established clearly
stated criteria for selecting the other
countries that could supply the United
States market with NRM: (a) France,
Hungary, Poland, and Yugoslavia
‘provided the United States with [NRM]
during the period 1975 through 1979
and present alternate sources’ and
Australia ‘was the source of material for
which import permits had been
requested during the time period’ and
(b) Each country did ‘impose adequate
controls over their production of
narcotic raw materials in adherence to
their obligations under the Single
Convention’.’’
DEA Response: DEA disagrees with
the commenters’ assessments that this
rule is inconsistent with the intent of
the 80/20 rule and international
resolutions. DEA finds that the
proposed rule is consistent with both
the 1979 resolution and the 80/20 rule.
Consistency with 1979 Resolution:
The text of the 1979 resolution
contained separate and distinct
operative language for Governments of
importing countries (i.e., the United
States) and Governments of producer
countries. The operative paragraph for
importing countries:
yshivers on PROD1PC62 with RULES
‘‘Urge[d] the Governments of the importing
countries that have not already done so to
take effective steps to support the traditional
supplier countries and to give those countries
all the practical assistance they can in order
to prevent the proliferation of sources of
production of narcotic raw materials for
export[.]’’ 6
Neither DEA nor the commenters
disagree that the United States meets the
first prong of this operative paragraph,
i.e., the support of ‘‘traditional supply
countries,’’ by providing India and
Turkey with access to at least 80 percent
of the United States market for
morphine contained in NRM. As has
been stated throughout this rule, DEA
remains committed to this obligation
through its continued support of the 80/
6 Resolution 1979/8 of the Economic and Social
Council. ‘‘Maintenance of a world-wide balance
between the supply of narcotic drugs and the
legitimate demand for those drugs for medical and
scientific purposes.’’
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15:18 Feb 05, 2008
Jkt 214001
20 rule. The commenter’s objections
would, therefore, fall under United
States’ obligations under the second
prong of this operative paragraph,
namely to give all practical assistance in
preventing the proliferation of
producing countries. Since it is not
refuted that the Government of Spain
has been engaged in the production of
NRM since 1974, prior to international
calls to prevent proliferation, DEA
concludes that the Government of Spain
is not a new or emerging participant in
the global production of NRM. The
addition of Spain to the 80/20 rule will
not result in a proliferation of producer
countries. DEA therefore concludes that
this action is consistent with the 1979
resolution.
Consistency with the 80/20 rule: As
stated in the proposed rulemaking and
reaffirmed in this final rule, DEA
concludes that adding Spain to the list
of countries authorized to export NRM
to the United States is consistent with
the 80/20 rule. Specifically, adding
Spain is consistent with the criteria
established by then-Acting
Administrator Mullen when
establishing Yugoslavia, France, Poland,
Hungary, and Australia as the list of
non-traditional suppliers in 1981. In the
1981 Final Rule, then-Acting
Administrator Mullen stated:
However, in view of the past commercial
relations with certain other countries as
sources of narcotic raw material supply and
the desirability of preserving alternate
sources of narcotic raw materials, it is
appropriate to allow certain specific
countries to compete for the U.S. narcotic
raw materials market on a limited basis.
These countries, France, Poland, Hungary
and Yugoslavia have provided the United
States with supplies of narcotic raw materials
during the period 1975 and 1979 and
represent appropriate alternate sources.
Australia is included as well since it was the
source of material for which import permits
had been requested during that time period.
In addition, we are presently persuaded that
the nations mentioned above impose
adequate controls over their production of
narcotic raw materials in adherence to their
obligations under the Single Convention. (46
FR 41775).
Then-Acting Administrator Mullen
reaffirmed DEA’s obligations to preserve
alternate sources of NRM for the United
States market. In an effort to determine
the sources from which NRM could be
derived, he established the following
two criteria in designating the list of
alternate sources: (1) The country had to
have supplied the United States with
NRM for a period of five years prior to
the resolution’s passage in 1979 and (2)
the country had to have imposed
adequate controls over the production of
NRM consistent with its obligations
PO 00000
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Sfmt 4700
6849
under the Single Convention. In his
decision, then-Acting Administrator
Mullen created an exception to the first
criterion; this exception allowed the
Government of Australia to be added to
the list of non-traditional suppliers.
Specifically, then-Acting Administrator
Mullen found that, if a country was not
the source of imports during the period
1975–1979, then the country had to be
a source from which DEA-registered
importers of NRM had requested
authority to import. Although Australia
did not export NRM to the United States
during the period 1975–1979, it was
added because DEA-registered NRM
importers had expressed interest in
importing from Australia and had
submitted to DEA the required
‘‘Application for Permit to Import
Controlled Substances for Domestic
and/or Scientific Purposes’’ (DEA–357)
from Australia.
Based on this exception, one could
conclude that Spain, despite not having
been a source of NRM to the United
States from 1975–1979, could qualify
consistent with the 80/20 rule if a DEAregistered importer had expressed its
interest in importing from Spain by
filing a DEA–357, requesting
authorization to do so. DEA notes,
however, that the filing of such an
application by a DEA-registered
importer at present would be
inconsistent with DEA regulations,
specifically the 80/20 rule, and would
therefore be impractical. Instead,
interest in importing NRM from Spain
arose through this rulemaking; DEA
notes that one DEA-registered NRM
importer expressed its interest in
importing NRM from Spain during the
comment period. DEA also notes that,
during routine annual discussions with
its five DEA-registered NRM importers
before the receipt of the petition from
the Government of Spain, the majority
expressed some degree of interest in
importing from Spain.
Neither the commenters nor DEA
disagree with the statements of fact
made by the Government of Spain that
it has implemented a system of
domestic controls for the handling of
NRM that are consistent with the Single
Convention; DEA concludes, as a result,
that the second criterion has been
satisfied.
DEA finds that adding Spain to the
list of non-traditional suppliers is
consistent with the criteria established
in 1981 by then-Acting Administrator
Mullen and is therefore consistent with
the 80/20 rule.
Cost of Narcotic Raw Materials
One DEA-registered importer of NRM
stated that DEA’s Notice of Proposed
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Federal Register / Vol. 73, No. 25 / Wednesday, February 6, 2008 / Rules and Regulations
Rulemaking ‘‘will do little or nothing to
improve adequacy of supply or the cost
of NRMs for the U.S.’’ The Government
of Australia, in its comments to the
DEA’s proposed rule stated that
‘‘Spain’s petition presents no evidence
to justify a need for change on the basis
of adequacy of supply nor the cost
effectiveness of that supply’’ and that
‘‘there is no real issue with cost.’’
Finally, the foreign opiate manufacturer
stated that there is no evidence that the
proposed rule would maintain costeffective supplies and that there is ‘‘no
suggestion that current supplies are not
cost effective.’’
DEA Response: DEA agrees that there
is no evidence provided in the petition
from Spain that the addition of Spain to
the 80/20 rule would lead to more costeffective supplies of NRM. This remains
an open question. DEA does not
routinely collect information relating to
the cost of NRM or the opiates
manufactured therefrom. Some of the
commenters, however, provided data
that demonstrate that the costs of NRM
have steadily declined over the last five
years and are presently at ‘‘record
lows.’’ For example, the DEA-registered
importer of NRM that objected to the
NPRM stated that the price of CPS–M
from Turkey was $660 per kilogram in
2001 and will be $300 per kilogram in
2007. The same commenter noted that
CPS–T was $825 per kilogram in 2001
and will be $500 per kilogram in 2007.
The foreign opiate manufacturer stated
that, ‘‘taking the United States supply
price in 2001 as a benchmark, the 2006
average price of Thebaine to the United
States has declined over 20%.’’ Given
the increasing demand for thebaine, the
foreign opiate manufacturer contends
that a decrease in price suggests a
‘‘robust competitive environment.’’
DEA disagrees with the implication
made by the Government of Australia,
however, in its statement that ‘‘Spain’s
assertion that its inclusion would
further an underlying policy objective of
the 80/20 Rule by ensuring an adequate
and reliable supply at a stable price is
based on a premise that prices of NRM
have not been stable.’’ DEA concludes
instead that the prices of NRM are
directly related to the global stocks of
these materials, which for more than the
last 5 years have been in excess of global
demand. For example, in the 2005 INCB
publication, ‘‘Narcotic Drugs: Estimated
World Requirements for 2006—
Statistics for 2004,’’ the INCB reported
that ‘‘global production of opiate raw
materials rich in morphine exceeded
global demand considerably during the
period 2002–2004.’’ For opiate raw
materials rich in thebaine, the INCB
reported that ‘‘the total supply
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15:18 Feb 05, 2008
Jkt 214001
(production and stocks) continued to be
above global demand also for thebainerich raw materials * * * and that the
balance between supply and demand
will continue to be positive.’’ DEA
therefore concludes that the decrease in
price noted by the commenters is more
a function of excess supply rather than
evidence of ‘‘robust competition,’’ for,
as noted, Australia supplies the vast
majority of the United States’ demand
for thebaine.
DEA further concludes that
maintaining cost-effective supplies of
NRM to the United States equates to
striking a global balance between supply
of and demand for NRM. For producer
countries such as India, Turkey,
Australia, France and Spain, this means
reducing areas of cultivation in times
when global supplies are in excess and
increasing production (to the extent
possible) if and when hardship arises in
a producer country that results in global
demand being in excess of supply. For
consumer countries, such as the United
States, this equates to: (1) Ensuring that
there are an adequate number of sources
from which to procure NRM during
times in which supplies are not in
excess, (2) communicating accurate
estimates of United States requirements
for NRM to authorized exporting
countries, and (3) working with the
international community, including the
INCB, to ensure a global balance
between supply and demand.
Replacing Yugoslavia With Spain
The Republic of Macedonia
(Macedonia) forwarded a letter prepared
by the only company licensed in
Macedonia to purchase poppy straw and
manufacture opiate alkaloids. The
company raised concerns regarding
DEA’s comment in the NPRM that ‘‘the
successor states to the former
Yugoslavia no longer produce NRM for
export.’’ The company disagreed with
this observation, stating that Macedonia
has been ‘‘enjoying the rights arising out
of the 80/20 rule for more than 25
years.’’ The company therefore insisted
that ‘‘Yugoslavia can only be replaced
on the list with its legitimate successor
state Macedonia.’’ A second commenter
stated that DEA’s proposed rule sought
to ‘‘replace Macedonia with Spain.’’
Finally, a third commenter stated that
DEA ignored ‘‘the position of its
[Yugoslavia’s] clear successor state,
namely Macedonia.’’
DEA Response: DEA disagrees with
those commenters that suggest that
Macedonia is the de facto successor to
Yugoslavia for purposes of the 80/20
rule. Macedonia became a sovereign
country only after the dissolution of
Yugoslavia. As a new country,
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Fmt 4700
Sfmt 4700
Macedonia cannot automatically replace
Yugoslavia in the 80/20 rule. Macedonia
is but one of five countries that were
created after the dissolution of
Yugoslavia in the early 1990s. Any one
of the five countries would be required
to petition DEA if it wished to be added
to the list of countries authorized to
export NRM. DEA would then be
required to review the merits of any
such petition in a manner consistent
with DEA’s review of the petition filed
by Spain.
DEA also disagrees with Macedonia’s
assessment that its manufacturers have
‘‘enjoyed’’ the rights arising from the 80/
20 rule for the last 25 years. The
company did not provide any statistical
data to demonstrate previous sales to
the United States or anticipated sales to
the United States. In this regard, DEA
conducted a review of import permits
issued for NRM over the last five years
and did not identify an occasion in
which a United States importer
requested authority to import NRM from
Macedonia. Instead, according to the
most recent statistics available from the
INCB (statistics for 2004), Macedonia
did not export opium, poppy straw, or
concentrate of poppy straw from 2002
through 2004. Instead, Macedonia
reported the exportation of small
quantities of morphine and codeine,
schedule II controlled substances whose
importation into the United States is
generally regarded as being prohibited
by DEA regulations unless specifically
requested in limited quantities for use
exclusively in scientific research (21
CFR 1312.13).
Conclusion
Based on the comments received,
statistical data on imports of NRM
collected and analyzed by DEA
pursuant to the Code of Federal
Regulations, and reports from the INCB,
DEA concludes that in order to continue
to ensure an adequate supply of NRM
necessary to meet the estimated
medical, industrial, scientific, and
research needs of the United States, for
lawful export requirements, and for the
maintenance of adequate stocks, it is
appropriate to add Spain to the list of
non-traditional countries permitted to
export NRM to the United States.
Regulatory Certifications
Regulatory Flexibility Act
The Deputy Assistant Administrator,
Office of Diversion Control, hereby
certifies that this rulemaking has been
drafted in accordance with the
Regulatory Flexibility Act (5 U.S.C.
601–612), that he has reviewed this
regulation, and by approving it certifies
E:\FR\FM\06FER1.SGM
06FER1
Federal Register / Vol. 73, No. 25 / Wednesday, February 6, 2008 / Rules and Regulations
that this regulation will not have a
significant economic impact on a
substantial number of small business
entities. This rule imposes no new costs
or burden on small entities. Rather, this
rule adds Spain to the list of nontraditional countries permitted to export
NRM to the United States, helping to
ensure that United States importers and
manufacturers will have access to, and
be able to procure, supplies of NRM to
meet legitimate United States medical,
scientific, research, and industrial
needs, to ensure maintenance of
adequate reserve stocks, and to meet
lawful export requirements.
Additionally, this rule provides DEA
registered importers with another source
from which to purchase NRM which are
utilized for the production of controlled
substances used in the United States for
medical purposes.
Executive Order 12866
The Deputy Assistant Administrator,
Office of Diversion Control, further
certifies that this rulemaking has been
drafted in accordance with the
principles in Executive Order 12866
Section 1(b). It has been determined that
this is a significant regulatory action.
Therefore, this action has been reviewed
by the Office of Management and
Budget.
Executive Order 12988
This rule meets the applicable
standards set forth in Sections 3(a) and
3(b)(2) of Executive Order 12988.
Executive Order 13132
This rule does not preempt or modify
any provision of State law; nor does it
impose enforcement responsibilities on
any State; nor does it diminish the
power of any State to enforce its own
laws. Accordingly, this rulemaking does
not have federalism implications
warranting the application of Executive
Order 13132.
yshivers on PROD1PC62 with RULES
Unfunded Mandates Reform Act of 1995
This rule will not result in the
expenditure by State, local, and tribal
governments, in the aggregate, or by the
private sector, of $120,000,000 or more
(adjusted for inflation) in any one year,
and will not significantly or uniquely
affect small governments. Therefore, no
actions were deemed necessary under
the provisions of the Unfunded
Mandates Reform Act of 1995.
Congressional Review Act
This rule is not a major rule as
defined by Section 804 of the Small
Business Regulatory Enforcement
Fairness Act of 1996 (Congressional
Review Act). This rule will not result in
VerDate Aug<31>2005
15:18 Feb 05, 2008
Jkt 214001
an annual effect on the economy of
$100,000,000 or more; a major increase
in costs or prices; or significant adverse
effects on competition, employment,
investment, productivity, innovation, or
on the ability of United States-based
companies to compete with foreignbased companies in domestic and
export markets.
List of Subjects in 21 CFR Part 1312
Administrative practice and
procedure, Drug traffic control, Exports,
Imports, Reporting and recordkeeping
requirements.
For the reasons set out above, 21 CFR
part 1312 is amended as follows:
I
PART 1312—IMPORTATION AND
EXPORTATION OF CONTROLLED
SUBSTANCES
1. The authority citation for part 1312
continues to read as follows:
I
Authority: 21 U.S.C. 952, 953, 954, 957,
958.
2. Section 1312.13 is amended by
revising paragraphs (f) and (g) to read as
follows:
I
§ 1312.13
Issuance of import permit.
*
*
*
*
*
(f) Notwithstanding paragraphs (a)(1)
and (a)(2) of this section, the
Administrator shall permit, pursuant to
section 1002(a)(1) or 1002(a)(2)(A) of the
Act (21 U.S.C. 952(a)(1) or (a)(2)(A)), the
importation of approved narcotic raw
material (opium, poppy straw and
concentrate of poppy straw) having as
its source:
(1) Turkey,
(2) India,
(3) Spain,
(4) France,
(5) Poland,
(6) Hungary, and
(7) Australia.
(g) At least eighty (80) percent of the
narcotic raw material imported into the
United States shall have as its original
source Turkey and India. Except under
conditions of insufficient supplies of
narcotic raw materials, not more than
twenty (20) percent of the narcotic raw
material imported into the United States
annually shall have as its source Spain,
France, Poland, Hungary and Australia.
Dated: January 30, 2008.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control.
[FR Doc. E8–2142 Filed 2–5–08; 8:45 am]
BILLING CODE 4410–09–P
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6851
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 180
[EPA–HQ–OPP–2007–0280; FRL–8346–9]
Clothianidin; Pesticide Tolerance
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
SUMMARY: This regulation establishes a
tolerance for residues of clothianidin in
or on sugar beet roots, tops and
molasses. Bayer CropScience requested
this tolerance under the Federal Food,
Drug, and Cosmetic Act (FFDCA).
DATES: This regulation is effective
February 6, 2008. Objections and
requests for hearings must be received
on or before April 7, 2008, and must be
filed in accordance with the instructions
provided in 40 CFR part 178 (see also
Unit I.C. of the SUPPLEMENTARY
INFORMATION).
EPA has established a
docket for this action under docket
identification (ID) number EPA–HQ–
OPP–2007–0280. To access the
electronic docket, go to https://
www.regulations.gov, select ‘‘Advanced
Search,’’ then ‘‘Docket Search.’’ Insert
the docket ID number where indicated
and select the ‘‘Submit’’ button. Follow
the instructions on the regulations.gov
website to view the docket index or
access available documents. All
documents in the docket are listed in
the docket index available in
regulations.gov. Although listed in the
index, some information is not publicly
available, e.g., Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Certain other material, such as
copyrighted material, is not placed on
the Internet and will be publicly
available only in hard copy form.
Publicly available docket materials are
available in the electronic docket at
https://www.regulations.gov, or, if only
available in hard copy, at the OPP
Regulatory Public Docket in Rm. S–
4400, One Potomac Yard (South Bldg.),
2777 S. Crystal Dr., Arlington, VA. The
Docket Facility is open from 8:30 a.m.
to 4 p.m., Monday through Friday,
excluding legal holidays. The Docket
Facility telephone number is (703) 305–
5805.
FOR FURTHER INFORMATION CONTACT:
Kable Bo Davis, Registration Division
(7505P), Office of Pesticide Programs,
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001; telephone number:
ADDRESSES:
E:\FR\FM\06FER1.SGM
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Agencies
[Federal Register Volume 73, Number 25 (Wednesday, February 6, 2008)]
[Rules and Regulations]
[Pages 6843-6851]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-2142]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
21 CFR Part 1312
[Docket No. DEA-282F]
RIN 1117-AB03
Authorized Sources of Narcotic Raw Materials
AGENCY: Drug Enforcement Administration (DEA), Department of Justice.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: The Drug Enforcement Administration (DEA) is amending the list
of non-traditional countries authorized to export narcotic raw
materials (NRM) to the United States by removing Yugoslavia and adding
Spain. This rule provides DEA registered importers with another
potential source from which to purchase NRM that are used in the
production of controlled substances for medical purposes in the United
States.
DATES: Effective Date: This rule is effective March 7, 2008.
FOR FURTHER INFORMATION CONTACT: Christine A. Sannerud, PhD, Chief,
Drug and Chemical Evaluation Section, Office of Diversion Control, Drug
Enforcement Administration, Washington, DC 20537, telephone (202) 307-
7183.
SUPPLEMENTARY INFORMATION:
Background and Legal Authority
DEA enforces the Comprehensive Drug Abuse Prevention and Control
Act of 1970, often referred to as the Controlled Substances Act (CSA)
and the Controlled Substances Import and Export Act (21 U.S.C. 801, et
seq.), as amended. DEA regulations implementing these statutes are
published in Title 21 of the Code of Federal Regulations (CFR), Parts
1300 to 1316. These regulations are designed to ensure that there is a
sufficient supply of controlled substances for legitimate medical,
scientific, research, and industrial purposes and to deter the
diversion of controlled substances to illegal purposes. The CSA and its
implementing regulations are consistent with United States treaty
obligations that, among other things, address the production, import,
and export of controlled substances.
Controlled Substances
Controlled substances are drugs that have a potential for abuse and
psychological and physical dependence, including opiates, stimulants,
depressants, hallucinogens, anabolic steroids, and drugs that are
immediate precursors of these classes of substances. DEA lists
controlled substances in 21 CFR Part 1308. The substances are divided
into five schedules. Schedule I substances have a high potential for
abuse and have no accepted medical use in treatment in the United
States. These substances may only be used for research, chemical
analysis, or manufacture of other drugs. Substances listed in schedules
II--V have accepted medical uses but also have potential for abuse and
psychological and physical dependence. Narcotic raw materials (opium,
poppy straw, and concentrate of poppy straw (CPS)) are in schedule II
and are the materials from which morphine, codeine, thebaine and
oripavine are extracted for purposes of manufacturing a number of
schedule II and III controlled substances.
Sources of Narcotic Raw Materials
In May 1979, the United Nations' Economic and Social Council
(ECOSOC) adopted Resolution 471, which called on importing countries
such as the United States to support traditional suppliers of NRM and
to limit imports from non-traditional supplying countries. The
resolution, which was reaffirmed by ECOSOC in 1981, was
[[Page 6844]]
adopted to limit overproduction of NRM, to restore a balance between
supply and demand, and to prevent diversion to illicit channels. The
United States, based on long-standing policy, does not cultivate or
produce NRM, but relies solely on opium, poppy straw, and CPS produced
in other countries for the NRM necessary to meet the legitimate medical
needs of the United States. In response to Resolution 471, on August
18, 1981, DEA published a final rule specifying certain source
countries of NRM (46 FR 41775); the rule is frequently referred to as
the 80/20 rule. Under the final rule, currently codified at 21 CFR
1312.13(f) and (g), NRM can be imported from only seven countries.
Traditional suppliers India and Turkey must be the source of at least
80 percent of the United States' requirement for NRM. Five non-
traditional supplier countries--France, Poland, Hungary, Australia, and
Yugoslavia--may be the source of not more than 20 percent. The 80/20
rule is calculated based on the amount of morphine alkaloid contained
in the NRM. The United States continues to reaffirm its support of the
original resolution by supporting similar resolutions each year at the
Commission on Narcotic Drugs.
Just as with DEA's 1979 Federal Register publication first
proposing the 80/20 rule (44 FR 33695), it is important to recite here
some of the central principles of Resolution 471, which remain crucial
today:
Noting that in recent years there has been considerable stepping
up of morphine producing capacity for export, leading to a situation
of substantial overproduction of opiates,
* * * * *
Recognizing that it is essential to bring about a proper balance
between the global supply and demand,
Taking note of the continued reliance placed by the world
community on countries constituting the traditional sources of
supply for its medical needs of opiate raw materials and the
positive response of these countries in meeting the world
requirements and their contribution in the maintenance of effective
control systems;
Bearing in mind that the treaties which establish this system
are based on the concept that the number of producers of narcotic
materials for export should be limited in order to facilitate
effective control; * * *
In view of these principles underlying Resolution 471, DEA stated
in proposing the 80/20 rule in 1979:
The United States is a significant importer of narcotic raw
materials. Its manufacturers account for one-third of the world
morphine manufacturing capacity, most of which is consumed within
the United States in the form of codeine.\1\ The worldwide over-
production of narcotic raw materials and [Resolution 471] make it
necessary for the United States to reevaluate past and present
narcotic policies.
---------------------------------------------------------------------------
\1\ Today, the United States remains a significant importer of
narcotic raw material. Its manufacturers currently account for one-
fourth of the world morphine manufacturing capacity, with roughly
two-thirds being utilized for the production of codeine, which is
consumed as either codeine or hydrocodone.
---------------------------------------------------------------------------
Historically, the United States has relied exclusively upon
imports of opium gum to manufacture our narcotic medical supplies
instead of cultivating opium poppies in the United States. The
rationale behind this 57-year-old policy, which foregoes [sic] U.S.
self-sufficiency, was to set an example to the world community to
refrain from overproduction and to limit the number of opium-
producing nations to a minimum.
[44 FR 33696, June 12, 1979]
The foregoing principles remain central to United States drug
control policy and this final rule amending the 80/20 rule.
Of the countries included in the 80/20 rule, India is the only
country that cultivates poppies for production of opium. All other
exporting countries use the CPS method of NRM production, a method that
allows the plant to go to seed; portions of the plant are then
processed into a concentrate. It is generally believed that CPS is less
divertible than opium. CPS may be rich in morphine (CPS-M), rich in
thebaine (CPS-T), or rich in oripavine (CPS-O). The United States
imports the majority of its CPS-M from Turkey, with Australia supplying
the vast majority of the balance. The vast majority of CPS-T and all
CPS-O are imported from Australia.
The 80/20 rule was established based on traditional import amounts
and on the United Nations resolution calling on member nations to
support traditional sources that have been reliable suppliers and to
take measures that curtail diversion. The United States allowed a
limited number of non-traditional suppliers to have access to the
United States market based on past commercial relationships and on the
desirability of preserving alternative sources. This approach was
consistent with the United Nations Resolution because it supported
India and Turkey and ensured an adequate and uninterrupted supply of
NRM while limiting the number of supplying countries. Over the last ten
years, pursuant to the 80/20 rule, DEA registered importers of NRM have
imported 90 percent of United States NRM requirements from traditional
suppliers India and Turkey. DEA continues its support of the intent of
the 80/20 rule.
On June 6, 2005, the Kingdom of Spain (hereinafter referred to as
Spain) petitioned DEA seeking to be added to the list of non-
traditional suppliers. Spain stated four reasons that granting its
petition would be consistent with United States interests:
The change would be consistent with the 80/20 rule because
it maintains India and Turkey as the two traditional supplier
countries, that is, Spain does not seek to be added to the list of
traditional suppliers.
The change would ensure adequate supplies of NRM.
The change would not result in diversion because Spain
maintains strict control and oversight over the cultivation and
distribution of NRM.
The change would allow DEA to monitor diversion and
maintain cost-effective supplies.
In its petition, Spain explained that in the early 1970s, Spanish
pharmaceutical firms sought authorization to cultivate opium poppies to
produce NRM. In 1973, the Government of Spain authorized a single firm,
Alcaliber, S.A., to cultivate, harvest, store, and prepare extracts
from the opium poppy. Spain is now the fifth largest cultivator of
opium poppies; Spain is the fourth largest producer of CPS and the
third largest exporter of CPS-M.\2\ Spain has ratified international
agreements to control production and commerce in opium products. As
stated in its petition, Spain has implemented a comprehensive
regulatory regime for controlling the cultivation, production, and
export of NRM in accordance with international treaty requirements. The
petition stated that this control ensures that NRM produced in Spain
are not diverted to illicit uses.
---------------------------------------------------------------------------
\2\ ``Narcotic Drugs: Estimated World Requirements for 2005--
Statistics for 2003'', Tables II and XIII; International Narcotics
Control Board (E/INCB/2004/2).
---------------------------------------------------------------------------
After review of the petition, DEA published a Notice of Proposed
Rulemaking (NPRM) in the Federal Register on October 4, 2006 (71 FR
58569) to amend the list of non-traditional countries authorized to
export NRM to the United States. Specifically, the proposed rule sought
to revise the list of non-traditional suppliers by removing Yugoslavia
and replacing it with Spain. At that time, DEA had determined that the
successor states to Yugoslavia no longer produced NRM for export beyond
Yugoslavia's prior border (e.g., Serbia and Montenegro reported exports
to the Republic of Macedonia (hereinafter referred to as Macedonia)
only). Therefore, DEA concluded that
[[Page 6845]]
replacing Yugoslavia with Spain would continue to limit the number of
non-traditional suppliers to the United States while ensuring the
availability of an adequate number of sources of NRM for United States
manufacturers. The proposed change would not otherwise affect the
implementation of the 80/20 rule.
Comments Received
Following publication of the Notice of Proposed Rulemaking on
October 4, 2006, DEA received a request for a 60-day extension to the
comment period. On December 1, 2006, DEA extended the comment period of
the proposed rule to January 3, 2007 (71 FR 69504).
During the comment period, DEA received 14 comments from 13
interested parties. Five comments were received from the following
countries: Australia, Spain, Macedonia, and Turkey. One of the comments
received from a foreign Government was a joint comment with a foreign
control board. Three comments were received from three DEA-registered
importers of NRM; one comment was received from a DEA-registered opiate
manufacturer; one comment was received from a non-DEA registered firm;
two comments were received from two foreign NRM manufacturers; and two
comments were received from one individual. As part of the above-listed
comments, DEA also received a request to extend the comment period, and
four requests for a hearing.
After the comment period had ended, DEA received an additional
comment from a foreign NRM manufacturer. This prompted two additional
late comments, one from the foreign control board which previously
commented on the NPRM and the other from the foreign government
associated with that foreign control board. Specifically, both
commenters sought clarification from DEA on the status of the late
comment, which DEA had administratively added to the docket. The
Administrative Procedure Act (APA) does not address the issue of late
comments, and the United States courts generally defer to federal
agencies in their handling of late comments. It is the policy of the
DEA that comments not properly filed, e.g., comments postmarked after
the close of a comment period, will not be considered by the agency in
its deliberative process. Accordingly, the late comment from the
foreign NRM manufacturer was not considered by DEA in this Final Rule.
All comments received during the comment period are summarized here and
discussed further below.
Comments in Support of DEA's NPRM
Four of the commenters supported the proposed rule. These
commenters included the Government of Spain, a DEA registered NRM
importer, one foreign NRM manufacturer, and a DEA-registered opiate
manufacturer. One of the DEA registrants commented that the need to
ensure an adequate number of sources of NRM for DEA-registered NRM
importers is ``most keenly felt in CPS-T and CPS-O, for which the U.S.
demand is rapidly growing and in which global supply sources to the
U.S. are currently quite limited.''
Comments Raising Concerns to DEA's NPRM
Nine of the commenters raised various concerns regarding the NPRM.
These commenters included the Government of Australia, the Government
of Macedonia, and the Government of Turkey; a foreign NRM control
board; two DEA-registered importers of NRM; one non-DEA-registered
firm; one foreign NRM manufacturer; and one individual.
Four commenters claimed that the proposed rule would exacerbate
current global oversupplies of NRM and therefore disrupt the balance
between the supply of and demand for NRM. Three commenters claimed that
the proposed rule was not consistent with the intent of the 80/20 rule
or international resolutions. Three commenters claimed that the
proposed rule was not necessary to assist the United States in
maintaining cost effective supplies of NRM. Three commenters questioned
DEA's decision to replace Yugoslavia with Spain.
The following additional concerns were raised. One commenter
believed that the addition of Spain to the list of non-traditional NRM
producing countries would lead to a proliferation of NRM-producing
countries. The commenter, however, did not provide further information
as to how this rulemaking would specifically lead to a proliferation of
NRM-producing countries. Additionally, one commenter claimed that Spain
has diversion occurring within its borders and that it could not be
proven that the addition of Spain to the list of non-traditional
countries would not lead to an increase in diversion within Spain.
While the commenter provided a general statement regarding the
diversion of controlled substances, the commenter did not provide any
specific evidence regarding the diversion of narcotic raw material
specifically cultivated for lawful purposes in Spain. Due to the lack
of substantiation for the claims discussed above, these comments are
not addressed further in this rulemaking.
Request for Hearing
Four commenters requested that DEA hold an administrative hearing
in this matter. Two of these commenters requested a hearing prior to
the issuance of the final rule. One of these commenters stated that a
hearing was appropriate ``given the gravity and complexity of the
issues involved.'' The other commenter stated that a hearing would
``provide interested parties with the fullest opportunity to make their
views known and have their positions considered.'' These commenters did
not proffer any specific information beyond that submitted in the
written comments, however, that would be brought to light if their
requests for a hearing were granted. DEA has determined that an oral
hearing prior to the issuance of this rule is unnecessary. The
amendment of the 80/20 rule to substitute one non-traditional country
for another that no longer exists in the form it did at the time of the
promulgation of the original rule does not represent a major change in
DEA policy or procedure. Moreover, DEA has carefully considered all of
the comments received in connection with the proposal, and finds that
the comments fully set forth the issues relevant to this rulemaking.
Based on information provided in the comments, information provided in
technical reports by the International Narcotics Control Board (INCB),
and information provided by U.S. importers of NRM pursuant to DEA
regulations, DEA has been able fully to address the relevant issues set
forth in the comments and has determined that conducting a hearing
would not materially add to the administrative record. DEA has
concluded, therefore, that such a hearing would be unnecessary.
Two other commenters requested a hearing following the issuance of
the final rule, if it is issued. Such a request does not conform
procedurally with traditional rulemaking procedures under the APA,
under which--if an agency holds a hearing in connection with a proposed
rule--it is held prior to the issuance of the final rule. Moreover,
neither the CSA nor DEA regulations provide for an administrative
hearing to ``appeal'' the promulgation of a final rule. Pursuant to 21
U.S.C. 877, exclusive jurisdiction for appeals of DEA final decisions
such as this rule rests with the United States Courts of Appeals.
Accordingly, the requests for a hearing if the final rule is issued are
denied.
[[Page 6846]]
Other Comments Received
One of the commenters wrote that if the proposal sought to change
the method by which the 80/20 rule was calculated, then the commenter
would object to the proposed rule. As noted previously, the 80/20 rule
is calculated based on the amount of morphine alkaloid contained in the
NRM. Since DEA's proposed rule and this rulemaking do not affect how
the 80/20 rule is calculated, this matter is not addressed further in
this rulemaking.
One commenter submitted two comments. One of these comments stated,
``So we are deciding who to allow to do the exporting of substances
that are used to make heroin? We allow this? And then kick down the
doors of terminally ill patients who smoke marijuana just to ease their
pain. * * *'' The other comment promoted the use of hallucinogens. NRM
imported into the United States pursuant to this rule are used to make
legitimate medicines that are used to treat pain, not to manufacture
heroin. Heroin production and the use of marijuana and hallucinogens
are not the subject of this rulemaking; these matters are therefore not
addressed further in this rulemaking.
Support for DEA's NPRM
Adequate Supply of NRM
Three commenters addressed the need to ensure adequate supplies of
NRM for United States markets. One commenter noted that the need to
ensure an adequate number of sources of NRM for DEA registered NRM
importers was ``most keenly felt in CPS-T and CPS-O, for which the U.S.
demand is rapidly growing and in which global supply sources to the
U.S. are currently quite limited.''
DEA Response: DEA agrees that United States sources of NRM are
limited based on data it collects quarterly from DEA registered
importers pursuant to 21 CFR 1304.31. The data collected in these
reports include the relative amounts of morphine, codeine, thebaine and
oripavine contained in each individual NRM import to the United States
as reported by each of the five DEA registered NRM importers. In
response to this comment, DEA conducted an analysis of the source of
each of the primary alkaloids available in current NRM: morphine,
thebaine and oripavine. DEA notes that, in 2006, imports of NRM had as
their source, four of the seven countries authorized to export NRM to
the United States, specifically India, Turkey, Australia and France.
United States importers have not imported NRM from Poland or Yugoslavia
since at least 1985, and imports from Hungary were minimal in the mid
to late 1990s and have ceased altogether since 2002. No imports from
Poland, Yugoslavia, or Hungary are anticipated in 2007. Since NRM
contain a mixture of these alkaloids, DEA's review of the NRM import
situation (below) is expressed in terms of the amount of morphine,
thebaine, and oripavine contained in imported NRM.
Morphine: Morphine is the principal alkaloid in Indian opium and
Turkish CPS-M and has historically been the principal alkaloid
extracted from NRM in the United States. Morphine continues to be
utilized in the United States for the manufacture of morphine-based
pharmaceutical products; the manufacture of codeine, which is utilized
to manufacture codeine-based pharmaceutical preparations and
hydrocodone; and the manufacture of hydromorphone. Based on an analysis
of information received for 2006, imports of NRM totaled 124,000 kg of
morphine (124.0 metric tons (MT)), having the following countries as
its source: Turkey (59.9 MT morphine; 48.3 percent), India (43.9 MT
morphine; 35.4 percent), and Australia (20.4 MT morphine; 16.5
percent).\3\ When reviewing imports of morphine over the last 10 years
(1997-2006), United States importers obtained commercial quantities of
morphine from India, Turkey, and Australia, with lesser amounts
obtained from France and Hungary. DEA concludes as a result that the
United States has at least three geographically distinct countries from
which morphine is obtained, each with large production capacity on
which the United States could rely if any of those countries were to
experience a hardship (i.e., crop failure, labor strife, etc.). Adding
Spain would provide DEA registered importers with a fourth country from
which to purchase NRM.
---------------------------------------------------------------------------
\3\ Percentages may not add to 100 percent due to rounding.
---------------------------------------------------------------------------
Thebaine: Thebaine is the principal alkaloid in CPS-T. CPS-T is
available to the United States market from Australia and France.
Thebaine is also present in Indian opium at approximately one sixth the
level of morphine, thus the amount of thebaine obtained from India is
directly related to the amount of morphine that United States importers
import from India. In the United States, thebaine is utilized for the
manufacture of oxycodone, a schedule II controlled substance. More
recently, oxycodone has been utilized for the manufacture of
oxymorphone, another schedule II controlled substance.
Oxycodone use in the United States has increased tremendously over
the last 10 years. For example, the aggregate production quota for
oxycodone, which represents the maximum amount that may be manufactured
in the United States to meet the estimated medical, industrial,
scientific, and research needs of the United States; for lawful export
requirements; and the maintenance of reserve stocks, has increased over
the last decade from 5,275 kg in 1997 to 49,200 kg in 2006. The large
increase in oxycodone use in the United States followed the approval
and marketing in 1995 of a high dose, single-entity, extended-release
drug formulation known as OxyContin. Although DEA remains concerned
over the diversion and abuse of OxyContin and other formulations that
contain high doses of potent schedule II controlled substances, the
Food and Drug Administration continues to advise DEA of double-digit
growth in the oxycodone market through 2008. This provides evidence
that the demand for thebaine-rich NRM that must be imported into the
United States for this purpose will also continue to increase.
When the same 2006 quarterly statistical import data was reviewed
for thebaine, DEA noted that 78.2 MT of thebaine was imported into the
United States in 2006, having as its source the following countries:
Australia (66.8 MT of thebaine; 85.4 percent), India (7.1 MT of
thebaine; (9.1 percent), and France (4.1 MT of thebaine; 5.2
percent).\4\ Thus, Australia was the source of 85 percent of United
States thebaine requirements in 2006.\5\ For comparison, in 2005, 73
percent of the 65.4 MT of thebaine imported into the United States had
Australia as it source, and, in 2004, 75 percent of the 66.8 MT were
imported from Australia. In 2007, United States importers have reported
their plans to import 92 percent of their thebaine requirements from
Australia; they planned to import the remaining 8 percent solely from
India.
---------------------------------------------------------------------------
\4\ Ibid.
\5\ As discussed previously, The 80/20 rule is calculated based
on the amount of morphine alkaloid contained in the NRM. As this
discussion relates to the amount of thebaine alkaloid in the NRM,
not morphine, the 85 percent obtained by the United States from
Australia does not violate principles of the 80/20 rule.
---------------------------------------------------------------------------
DEA notes that Australia has a stellar record in providing
thebaine-rich NRM to the United States, with little (if any) record of
diversion. DEA further notes that the United States and Australia have
excellent relations in this area, and contrary to comments made by some
commenters to this NPRM, DEA's proposed rule and this final rule in no
[[Page 6847]]
way suggest that Australia has ``not ensured an adequate and
uninterrupted supply'' of NRM to the United States. DEA remains
mindful, however, of the potential impact of a hardship (i.e., crop
failure, labor strife, etc.) in Australia that could lead to a
temporary lack of availability of thebaine to the United States market.
In this circumstance, the United States would be required to obtain
much larger volumes of NRM from either India or France in order to meet
thebaine demand. Although France has demonstrated the capability of
exporting up to 16 MT of thebaine in a single year to the United
States, India's capacity to export thebaine, as mentioned above, is
directly related to the amount of morphine that importers wish to
import from India consistent with the 80/20 rule. Therefore, importing
vast quantities of Indian opium to meet United States thebaine demands
would be impractical because it would result in the importation into
the United States of excessive amounts of morphine, which could then be
the subject of diversion and abuse. Thus, the amount of thebaine that
could be derived from India, consistent with United States requirements
for morphine contained in Indian opium, is likely to be 6-8 MT
annually. DEA concludes that the United States has limited sources from
which to obtain thebaine derived from NRM. The United States relies on
three countries for thebaine, but two of these countries have a limited
capacity to support the increasing size of the United States' market
for thebaine. DEA notes that, in 2004, the Government of Spain reported
for the first time commercial production of CPS-T, so Spain would
represent a fourth country from which CPS-T could be imported. As a
result, this rule will provide DEA registered importers with another
source from which to purchase CPS-T for the production of medicines.
Oripavine: Oripavine, a schedule II controlled substance, is the
principal alkaloid found in Australian CPS-O and is a minor constituent
in French CPS-T. Oripavine is becoming an increasingly important
intermediate in the United States for the manufacture of buprenorphine,
a schedule III controlled substance, oxymorphone, and a number of
controlled and non-controlled substances referred to generally as
``opiate antagonists'' (naltrexone for example, and its derivatives).
Using the same import data, DEA notes that, in 2006, 9.7 MT of
oripavine was imported into the United States having Australia as its
source, virtually 100 percent of the United States' oripavine
requirements. In 2005, 4.1 MT were imported from Australia and in 2004,
9.4 MT were imported with roughly 86 percent imported from Australia.
United States importers have reported their plans to import 100 percent
of the 9.7 MT of oripavine from Australia in 2007. DEA therefore
concludes that the United States has limited sources from which to
obtain oripavine derived from NRM.
Objections to DEA's NPRM
Global Oversupply of Narcotic Raw Materials
The Government of Australia's primary concern regarding DEA's
proposed rule is that this rule would ``exacerbate global oversupply''
of NRM. In its comment, the Government of Australia pointed to
statistical data published by the INCB in its report, ``Narcotic Drugs:
Estimated World Requirements for 2006--Statistics for 2004,'' which the
Government of Australia characterized as demonstrating that global
production of both morphine-rich and thebaine-rich NRM have been in
excess of global utilization since at least 2001. As a result of
overproduction, the Government of Australia argued, global supplies
have increased.
The DEA-registered NRM importer stated that ``Alcaliber [the sole
Spanish poppy cultivator] made a significant investment in capacity,
dramatically increased production contributing significantly to global
overproduction and excess stocks, and now wants access to the U.S.
market to allow it to increase production further to help recover its
investment.'' The importer further stated that the Notice of Proposed
Rulemaking sent the message that ``If a country adds production
capacity, uses it aggressively and thereby contributes to the world's
build up of excess stocks, the U.S. will accommodate this behavior and
reward it with access to the U.S. market. The U.S. will simply delete a
smaller producer from the list.'' This commenter also stated that
``Spain was arguably the primary source of this build up in excess
morphine stocks.''
Finally, the foreign opiate manufacturer stated that ``Spain's
rapid expansion of its domestic industry, its aggressive approach to
building export markets, its building of clearly excessive stockpiles
and capacity, and supply into a market already in over-supply is not *
* * broadly in accordance with the obligations under the Single
Convention, or the Resolutions.''
DEA Response: DEA disagrees that Spain is the ``primary'' source of
any build-up of global excesses in morphine stocks. Instead, DEA
concludes that all countries that produce NRM contribute to the current
global excess of NRM.
Among many of the requirements of NRM-producing countries, in
accordance with the Single Convention on Narcotic Drugs, 1961, is a
requirement to provide annual statistics to the INCB, including
estimated amounts of NRM to be cultivated and the amount of NRM to be
produced therefrom. The INCB utilizes these estimates along with other
statistical data it collects, in accordance with the Single Convention,
to monitor and analyze the global supply of and demand for NRM. The
results of this analysis are published in a technical report series,
which in 2004 was entitled, ``Narcotic Drugs: Estimated World
Requirements for 2006; Statistics for 2003.'' The analysis conducted by
the INCB and the statistical reports published continue to be an
excellent resource for governments of consumer countries such as the
United States. A review of this report series for 2004 and 2005 was
conducted with relevant statistical data provided in Tables 1 and 2.
Analysis for Morphine-Rich Poppies
Table 1.--``Global Cultivation of Morphine-Rich Poppies (Hectares) for Licit Purposes Other Than Production of
Opium''
----------------------------------------------------------------------------------------------------------------
2005 (ha- 2006 (ha-
Country 2003 (ha) 2004 (ha) est.) est.)
----------------------------------------------------------------------------------------------------------------
Australia................................................... 9,811 6,644 6,700 4,900
People's Republic of China.................................. 1,250 1,000 1,300 1,200
Czech Republic.............................................. 21,045 16,030 25,000 38,000
France...................................................... 7,919 8,312 8,500 9,100
Hungary..................................................... 2,937 7,084 14,000 12,000
Slovakia.................................................... 332 326 550 ...........
[[Page 6848]]
Spain....................................................... 5,732 5,986 7,002 6,002
Republic of Macedonia....................................... 51 91 1,500 1,500
Turkey...................................................... 99,430 30,343 70,000 70,000
United Kingdom.............................................. 1,534 1,534 1,500 ...........
---------------------------------------------------
Total................................................... 150,041 77,350 136,052 142,702
----------------------------------------------------------------------------------------------------------------
Neither DEA, nor any commenter, identified a single instance in
these reports in which the INCB raised concerns over Spain's purported
role in the global excess of production and the resulting oversupply of
NRM presently on hand. According to this publication, Spain was one of
eleven countries that cultivated morphine-rich poppies in 2003 for
licit pharmaceutical purposes (i.e. non-culinary use). Spain planted
5,732 hectares of poppies and produced roughly 4.7 percent of the
world's morphine-rich poppy straw. Spain's share of world production of
poppy straw increased in 2004 to 10.7 percent; the increase was
attributed to both an increase in 2004 acreage sown in Spain and a
large decrease in acreage sown by the primary cultivator of poppies for
this purpose, Turkey. Estimates for the ``area to be cultivated'' for
2005 and 2006 suggest that Spain will be responsible for 5.1 percent of
the area under cultivation and had plans to decrease its area under
cultivation in 2006 to 4.2 percent.
Although Spain remains one of the five largest cultivators of
morphine-rich poppies in the world, DEA concludes that Spain, like all
other producer and consumer countries, contributes to what the INCB
qualifies as a ``high'' level of stocks of raw materials rich in
morphine.
Analysis of Thebaine-Rich Poppies
Table 2.--``Global Cultivation of Thebaine-Rich Poppies (Hectares) for Licit Purposes Other Than Production of
Opium''
----------------------------------------------------------------------------------------------------------------
2005 (ha- 2006 (ha-
Country 2003 (ha) 2004 (ha) est.) est.)
----------------------------------------------------------------------------------------------------------------
Australia................................................... 7,637 5,578 6,500 5,300
People's Republic of China.................................. 34 ........... 40 50
France...................................................... 1,499 1,007 1,100 1,000
Spain....................................................... ........... 996 500 1,000
---------------------------------------------------
Total................................................... 9,170 7,581 8,140 7,350
----------------------------------------------------------------------------------------------------------------
Australia is the principal cultivator of thebaine-rich poppies and
is responsible for the vast majority of thebaine-rich CPS that is
produced and imported into the United States. Although the INCB notes
that production of thebaine-rich NRM exceeded demand substantially
until 2002, DEA notes that the primary cultivators, Australia and
France, began decreasing areas under cultivation in 2003 and have made
significant decreases since that time in order to bring production in
line with utilization. Although Spain noted cultivation of thebaine-
rich poppies for the first time in 2004, it is not responsible for
excess production that resulted in excess supplies before then.
Consistency With the 80/20 Rule and International Resolutions
As stated in DEA's Notice of Proposed Rulemaking, the 80/20 rule
was promulgated following a resolution adopted by the United Nations'
Economic and Social Council (ECOSOC) in 1979. In response to the
resolution in 1979, DEA published an Advance Notice of Proposed
Rulemaking (44 FR 33695, June 12, 1979) and then a Notice of Proposed
Rulemaking (45 FR 9289, February 12, 1980). The comments resulting from
the Notice of Proposed Rulemaking led to an administrative hearing. On
August 18, 1981, DEA published a final rule promulgating the 80/20 rule
(46 FR 41775).
Objections to the current Notice of Proposed Rulemaking pointed to
specific comments in the 1979 resolution, the Notice of Proposed
Rulemaking, the transcript of the administrative hearing, and
considerations made by then-Acting Administrator Francis Mullen, Jr.,
in DEA's 1981 Final Rule.
The foreign opiate manufacturer stated that the 1979 ECOSOC
resolution called on ``importing countries to * * * take effective
steps to support their traditional supplier countries'' and urged
``major producing and manufacturing countries to which have set up
[sic] additional capacity in recent years to take effective measures to
restrict substantially their production levels to assure a lasting
balance between supply and demand and to prevent drug diversion to
illicit channels.'' The commenter believed that ``[a]llowing Spain to
now enter the market directly contradicts and undermines the objective
of the Current 80/20 Rule, and rewards a country for engaging in the
very conduct the Current 80/20 Rule, and the Resolutions, were intended
to discourage or stop.''
The DEA-registered NRM importer who filed objections to the NPRM
provided a summary of the determinations of fact made by Francis Young,
the Administrative Law Judge (ALJ) who presided over the hearing in
1980; these findings were adopted by then-Acting Administrator Mullen
when the final rule was promulgated. The DEA-registered importer
provided the following summary of ALJ Young's determinations of fact:
``(1) DEA could lawfully promulgate the regulatory amendments limiting
the importation of narcotic raw materials; (2) the Administrator of DEA
could lawfully
[[Page 6849]]
require that a major portion of the [NRM] imported into the United
States be produced in India and Turkey while permitting the remainder
of the U.S. needs to be imported from other countries which maintain
adequate control; (3) such allocation would be in harmony with U.S.
trade agreements and would not be inconsistent with Resolution 471 and
497; and (4) DEA staff should determine an allocation ratio based upon
world market shares during a recent representative period.'' This
commenter further noted that the 1981 final rule ``established clearly
stated criteria for selecting the other countries that could supply the
United States market with NRM: (a) France, Hungary, Poland, and
Yugoslavia `provided the United States with [NRM] during the period
1975 through 1979 and present alternate sources' and Australia `was the
source of material for which import permits had been requested during
the time period' and (b) Each country did `impose adequate controls
over their production of narcotic raw materials in adherence to their
obligations under the Single Convention'.''
DEA Response: DEA disagrees with the commenters' assessments that
this rule is inconsistent with the intent of the 80/20 rule and
international resolutions. DEA finds that the proposed rule is
consistent with both the 1979 resolution and the 80/20 rule.
Consistency with 1979 Resolution: The text of the 1979 resolution
contained separate and distinct operative language for Governments of
importing countries (i.e., the United States) and Governments of
producer countries. The operative paragraph for importing countries:
``Urge[d] the Governments of the importing countries that have
not already done so to take effective steps to support the
traditional supplier countries and to give those countries all the
practical assistance they can in order to prevent the proliferation
of sources of production of narcotic raw materials for export[.]''
\6\
---------------------------------------------------------------------------
\6\ Resolution 1979/8 of the Economic and Social Council.
``Maintenance of a world-wide balance between the supply of narcotic
drugs and the legitimate demand for those drugs for medical and
scientific purposes.''
Neither DEA nor the commenters disagree that the United States
meets the first prong of this operative paragraph, i.e., the support of
``traditional supply countries,'' by providing India and Turkey with
access to at least 80 percent of the United States market for morphine
contained in NRM. As has been stated throughout this rule, DEA remains
committed to this obligation through its continued support of the 80/20
rule. The commenter's objections would, therefore, fall under United
States' obligations under the second prong of this operative paragraph,
namely to give all practical assistance in preventing the proliferation
of producing countries. Since it is not refuted that the Government of
Spain has been engaged in the production of NRM since 1974, prior to
international calls to prevent proliferation, DEA concludes that the
Government of Spain is not a new or emerging participant in the global
production of NRM. The addition of Spain to the 80/20 rule will not
result in a proliferation of producer countries. DEA therefore
concludes that this action is consistent with the 1979 resolution.
Consistency with the 80/20 rule: As stated in the proposed
rulemaking and reaffirmed in this final rule, DEA concludes that adding
Spain to the list of countries authorized to export NRM to the United
States is consistent with the 80/20 rule. Specifically, adding Spain is
consistent with the criteria established by then-Acting Administrator
Mullen when establishing Yugoslavia, France, Poland, Hungary, and
Australia as the list of non-traditional suppliers in 1981. In the 1981
Final Rule, then-Acting Administrator Mullen stated:
However, in view of the past commercial relations with certain
other countries as sources of narcotic raw material supply and the
desirability of preserving alternate sources of narcotic raw
materials, it is appropriate to allow certain specific countries to
compete for the U.S. narcotic raw materials market on a limited
basis. These countries, France, Poland, Hungary and Yugoslavia have
provided the United States with supplies of narcotic raw materials
during the period 1975 and 1979 and represent appropriate alternate
sources. Australia is included as well since it was the source of
material for which import permits had been requested during that
time period. In addition, we are presently persuaded that the
nations mentioned above impose adequate controls over their
production of narcotic raw materials in adherence to their
obligations under the Single Convention. (46 FR 41775).
Then-Acting Administrator Mullen reaffirmed DEA's obligations to
preserve alternate sources of NRM for the United States market. In an
effort to determine the sources from which NRM could be derived, he
established the following two criteria in designating the list of
alternate sources: (1) The country had to have supplied the United
States with NRM for a period of five years prior to the resolution's
passage in 1979 and (2) the country had to have imposed adequate
controls over the production of NRM consistent with its obligations
under the Single Convention. In his decision, then-Acting Administrator
Mullen created an exception to the first criterion; this exception
allowed the Government of Australia to be added to the list of non-
traditional suppliers. Specifically, then-Acting Administrator Mullen
found that, if a country was not the source of imports during the
period 1975-1979, then the country had to be a source from which DEA-
registered importers of NRM had requested authority to import. Although
Australia did not export NRM to the United States during the period
1975-1979, it was added because DEA-registered NRM importers had
expressed interest in importing from Australia and had submitted to DEA
the required ``Application for Permit to Import Controlled Substances
for Domestic and/or Scientific Purposes'' (DEA-357) from Australia.
Based on this exception, one could conclude that Spain, despite not
having been a source of NRM to the United States from 1975-1979, could
qualify consistent with the 80/20 rule if a DEA-registered importer had
expressed its interest in importing from Spain by filing a DEA-357,
requesting authorization to do so. DEA notes, however, that the filing
of such an application by a DEA-registered importer at present would be
inconsistent with DEA regulations, specifically the 80/20 rule, and
would therefore be impractical. Instead, interest in importing NRM from
Spain arose through this rulemaking; DEA notes that one DEA-registered
NRM importer expressed its interest in importing NRM from Spain during
the comment period. DEA also notes that, during routine annual
discussions with its five DEA-registered NRM importers before the
receipt of the petition from the Government of Spain, the majority
expressed some degree of interest in importing from Spain.
Neither the commenters nor DEA disagree with the statements of fact
made by the Government of Spain that it has implemented a system of
domestic controls for the handling of NRM that are consistent with the
Single Convention; DEA concludes, as a result, that the second
criterion has been satisfied.
DEA finds that adding Spain to the list of non-traditional
suppliers is consistent with the criteria established in 1981 by then-
Acting Administrator Mullen and is therefore consistent with the 80/20
rule.
Cost of Narcotic Raw Materials
One DEA-registered importer of NRM stated that DEA's Notice of
Proposed
[[Page 6850]]
Rulemaking ``will do little or nothing to improve adequacy of supply or
the cost of NRMs for the U.S.'' The Government of Australia, in its
comments to the DEA's proposed rule stated that ``Spain's petition
presents no evidence to justify a need for change on the basis of
adequacy of supply nor the cost effectiveness of that supply'' and that
``there is no real issue with cost.'' Finally, the foreign opiate
manufacturer stated that there is no evidence that the proposed rule
would maintain cost-effective supplies and that there is ``no
suggestion that current supplies are not cost effective.''
DEA Response: DEA agrees that there is no evidence provided in the
petition from Spain that the addition of Spain to the 80/20 rule would
lead to more cost-effective supplies of NRM. This remains an open
question. DEA does not routinely collect information relating to the
cost of NRM or the opiates manufactured therefrom. Some of the
commenters, however, provided data that demonstrate that the costs of
NRM have steadily declined over the last five years and are presently
at ``record lows.'' For example, the DEA-registered importer of NRM
that objected to the NPRM stated that the price of CPS-M from Turkey
was $660 per kilogram in 2001 and will be $300 per kilogram in 2007.
The same commenter noted that CPS-T was $825 per kilogram in 2001 and
will be $500 per kilogram in 2007. The foreign opiate manufacturer
stated that, ``taking the United States supply price in 2001 as a
benchmark, the 2006 average price of Thebaine to the United States has
declined over 20%.'' Given the increasing demand for thebaine, the
foreign opiate manufacturer contends that a decrease in price suggests
a ``robust competitive environment.''
DEA disagrees with the implication made by the Government of
Australia, however, in its statement that ``Spain's assertion that its
inclusion would further an underlying policy objective of the 80/20
Rule by ensuring an adequate and reliable supply at a stable price is
based on a premise that prices of NRM have not been stable.'' DEA
concludes instead that the prices of NRM are directly related to the
global stocks of these materials, which for more than the last 5 years
have been in excess of global demand. For example, in the 2005 INCB
publication, ``Narcotic Drugs: Estimated World Requirements for 2006--
Statistics for 2004,'' the INCB reported that ``global production of
opiate raw materials rich in morphine exceeded global demand
considerably during the period 2002-2004.'' For opiate raw materials
rich in thebaine, the INCB reported that ``the total supply (production
and stocks) continued to be above global demand also for thebaine-rich
raw materials * * * and that the balance between supply and demand will
continue to be positive.'' DEA therefore concludes that the decrease in
price noted by the commenters is more a function of excess supply
rather than evidence of ``robust competition,'' for, as noted,
Australia supplies the vast majority of the United States' demand for
thebaine.
DEA further concludes that maintaining cost-effective supplies of
NRM to the United States equates to striking a global balance between
supply of and demand for NRM. For producer countries such as India,
Turkey, Australia, France and Spain, this means reducing areas of
cultivation in times when global supplies are in excess and increasing
production (to the extent possible) if and when hardship arises in a
producer country that results in global demand being in excess of
supply. For consumer countries, such as the United States, this equates
to: (1) Ensuring that there are an adequate number of sources from
which to procure NRM during times in which supplies are not in excess,
(2) communicating accurate estimates of United States requirements for
NRM to authorized exporting countries, and (3) working with the
international community, including the INCB, to ensure a global balance
between supply and demand.
Replacing Yugoslavia With Spain
The Republic of Macedonia (Macedonia) forwarded a letter prepared
by the only company licensed in Macedonia to purchase poppy straw and
manufacture opiate alkaloids. The company raised concerns regarding
DEA's comment in the NPRM that ``the successor states to the former
Yugoslavia no longer produce NRM for export.'' The company disagreed
with this observation, stating that Macedonia has been ``enjoying the
rights arising out of the 80/20 rule for more than 25 years.'' The
company therefore insisted that ``Yugoslavia can only be replaced on
the list with its legitimate successor state Macedonia.'' A second
commenter stated that DEA's proposed rule sought to ``replace Macedonia
with Spain.'' Finally, a third commenter stated that DEA ignored ``the
position of its [Yugoslavia's] clear successor state, namely
Macedonia.''
DEA Response: DEA disagrees with those commenters that suggest that
Macedonia is the de facto successor to Yugoslavia for purposes of the
80/20 rule. Macedonia became a sovereign country only after the
dissolution of Yugoslavia. As a new country, Macedonia cannot
automatically replace Yugoslavia in the 80/20 rule. Macedonia is but
one of five countries that were created after the dissolution of
Yugoslavia in the early 1990s. Any one of the five countries would be
required to petition DEA if it wished to be added to the list of
countries authorized to export NRM. DEA would then be required to
review the merits of any such petition in a manner consistent with
DEA's review of the petition filed by Spain.
DEA also disagrees with Macedonia's assessment that its
manufacturers have ``enjoyed'' the rights arising from the 80/20 rule
for the last 25 years. The company did not provide any statistical data
to demonstrate previous sales to the United States or anticipated sales
to the United States. In this regard, DEA conducted a review of import
permits issued for NRM over the last five years and did not identify an
occasion in which a United States importer requested authority to
import NRM from Macedonia. Instead, according to the most recent
statistics available from the INCB (statistics for 2004), Macedonia did
not export opium, poppy straw, or concentrate of poppy straw from 2002
through 2004. Instead, Macedonia reported the exportation of small
quantities of morphine and codeine, schedule II controlled substances
whose importation into the United States is generally regarded as being
prohibited by DEA regulations unless specifically requested in limited
quantities for use exclusively in scientific research (21 CFR 1312.13).
Conclusion
Based on the comments received, statistical data on imports of NRM
collected and analyzed by DEA pursuant to the Code of Federal
Regulations, and reports from the INCB, DEA concludes that in order to
continue to ensure an adequate supply of NRM necessary to meet the
estimated medical, industrial, scientific, and research needs of the
United States, for lawful export requirements, and for the maintenance
of adequate stocks, it is appropriate to add Spain to the list of non-
traditional countries permitted to export NRM to the United States.
Regulatory Certifications
Regulatory Flexibility Act
The Deputy Assistant Administrator, Office of Diversion Control,
hereby certifies that this rulemaking has been drafted in accordance
with the Regulatory Flexibility Act (5 U.S.C. 601-612), that he has
reviewed this regulation, and by approving it certifies
[[Page 6851]]
that this regulation will not have a significant economic impact on a
substantial number of small business entities. This rule imposes no new
costs or burden on small entities. Rather, this rule adds Spain to the
list of non-traditional countries permitted to export NRM to the United
States, helping to ensure that United States importers and
manufacturers will have access to, and be able to procure, supplies of
NRM to meet legitimate United States medical, scientific, research, and
industrial needs, to ensure maintenance of adequate reserve stocks, and
to meet lawful export requirements. Additionally, this rule provides
DEA registered importers with another source from which to purchase NRM
which are utilized for the production of controlled substances used in
the United States for medical purposes.
Executive Order 12866
The Deputy Assistant Administrator, Office of Diversion Control,
further certifies that this rulemaking has been drafted in accordance
with the principles in Executive Order 12866 Section 1(b). It has been
determined that this is a significant regulatory action. Therefore,
this action has been reviewed by the Office of Management and Budget.
Executive Order 12988
This rule meets the applicable standards set forth in Sections 3(a)
and 3(b)(2) of Executive Order 12988.
Executive Order 13132
This rule does not preempt or modify any provision of State law;
nor does it impose enforcement responsibilities on any State; nor does
it diminish the power of any State to enforce its own laws.
Accordingly, this rulemaking does not have federalism implications
warranting the application of Executive Order 13132.
Unfunded Mandates Reform Act of 1995
This rule will not result in the expenditure by State, local, and
tribal governments, in the aggregate, or by the private sector, of
$120,000,000 or more (adjusted for inflation) in any one year, and will
not significantly or uniquely affect small governments. Therefore, no
actions were deemed necessary under the provisions of the Unfunded
Mandates Reform Act of 1995.
Congressional Review Act
This rule is not a major rule as defined by Section 804 of the
Small Business Regulatory Enforcement Fairness Act of 1996
(Congressional Review Act). This rule will not result in an annual
effect on the economy of $100,000,000 or more; a major increase in
costs or prices; or significant adverse effects on competition,
employment, investment, productivity, innovation, or on the ability of
United States-based companies to compete with foreign-based companies
in domestic and export markets.
List of Subjects in 21 CFR Part 1312
Administrative practice and procedure, Drug traffic control,
Exports, Imports, Reporting and recordkeeping requirements.
0
For the reasons set out above, 21 CFR part 1312 is amended as follows:
PART 1312--IMPORTATION AND EXPORTATION OF CONTROLLED SUBSTANCES
0
1. The authority citation for part 1312 continues to read as follows:
Authority: 21 U.S.C. 952, 953, 954, 957, 958.
0
2. Section 1312.13 is amended by revising paragraphs (f) and (g) to
read as follows:
Sec. 1312.13 Issuance of import permit.
* * * * *
(f) Notwithstanding paragraphs (a)(1) and (a)(2) of this section,
the Administrator shall permit, pursuant to section 1002(a)(1) or
1002(a)(2)(A) of the Act (21 U.S.C. 952(a)(1) or (a)(2)(A)), the
importation of approved narcotic raw material (opium, poppy straw and
concentrate of poppy straw) having as its source:
(1) Turkey,
(2) India,
(3) Spain,
(4) France,
(5) Poland,
(6) Hungary, and
(7) Australia.
(g) At least eighty (80) percent of the narcotic raw material
imported into the United States shall have as its original source
Turkey and India. Except under conditions of insufficient supplies of
narcotic raw materials, not more than twenty (20) percent of the
narcotic raw material imported into the United States annually shall
have as its source Spain, France, Poland, Hungary and Australia.
Dated: January 30, 2008.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control.
[FR Doc. E8-2142 Filed 2-5-08; 8:45 am]
BILLING CODE 4410-09-P