Correction of Code of Federal Regulations: Removal of Temporary Listing of Benzylfentanyl and Thenylfentanyl as Controlled Substances, 37300-37301 [2010-15529]
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37300
Federal Register / Vol. 75, No. 124 / Tuesday, June 29, 2010 / Rules and Regulations
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
21 CFR Part 1308
[Docket No. DEA–313F]
RIN 1117–AB26
Correction of Code of Federal
Regulations: Removal of Temporary
Listing of Benzylfentanyl and
Thenylfentanyl as Controlled
Substances
AGENCY: Drug Enforcement
Administration (DEA), Department of
Justice
ACTION: Final rule.
SUMMARY: This rulemaking corrects Title
21 Code of Federal Regulations (CFR) by
deleting regulations which list the
substances benzylfentanyl and
thenylfentanyl as being temporarily
subject to schedule I controls under the
emergency scheduling provisions of the
Controlled Substances Act (CSA). The
temporary scheduling of benzylfentanyl
and thenylfentanyl expired on
November 29, 1986. DEA determined
that these compounds were both
essentially inactive, with no evidence of
abuse potential. As such, these
compounds are no longer schedule I
controlled substances and all references
to these compounds are being deleted
from DEA regulations.
DATES: This rulemaking becomes
effective June 29, 2010.
FOR FURTHER INFORMATION CONTACT:
Christine A. Sannerud, PhD, Chief, Drug
and Chemical Evaluation Section, Office
of Diversion Control, Drug Enforcement
Administration, 8701 Morrissette Drive,
Springfield, VA 22152 at (202) 307–
7183.
The CSA
was amended by the Comprehensive
Crime Control Act of 1984 (Pub. L.98–
473) which became effective on October
12, 1984. This Act included a provision
(21 U.S.C. 811(h)) which allows the
DEA Administrator to place a substance,
on a temporary basis, into schedule I
when necessary to avoid an imminent
hazard to the public safety. This
emergency scheduling authority permits
scheduling a substance that is not
currently controlled, is being abused,
and is a risk to the public health while
the formal rulemaking procedures
(21 U.S.C. 811) described in the CSA are
being conducted. A temporary
scheduling order may be issued for one
wwoods2 on DSK1DXX6B1PROD with RULES
SUPPLEMENTARY INFORMATION:
year with a possible extension of up to
six months if formal scheduling
procedures have been initiated. The
proposal and order are published in the
Federal Register as are the proposals
and orders for formal scheduling. The
emergency scheduling authority was
given to DEA in an effort to streamline
the scheduling process in response to
the growing problem of controlled
substance analogues (‘‘designer drugs’’).
On October 29, 1985, DEA published
a Final Rule (50 FR 43698) which
temporarily placed Acetyl-alphamethylfentanyl, Alphamethylthiofentanyl, Betahydroxyfentanyl, Beta-hydroxy-3methylfentanyl, 3-Methylthiofentanyl,
Thiofentanyl, Benzylfentanyl and
Thenylfentanyl into schedule I of the
CSA. This control action became
effective on November 29, 1985.
These substances were emergency
scheduled based on their appearance in
the illicit market, their similarity in
chemical structure to that of controlled
substances, and the likelihood that they
would produce pharmacological effects
similar to those of prototypic schedule
I or II substances. Often there is no
biological data available prior to the
emergency control of illicitly produced
and abused substances. Therefore,
information derived from structureactivity relationship considerations
plays an important role in emergency
scheduling. To keep an emergency
scheduled substance in schedule I, DEA
must initiate traditional scheduling
procedures (21 U.S.C. 811) for that
substance during the one year period in
which it is emergency controlled and
complete the action before the
expiration of 18 months. The time
limitations of emergency scheduling
underscore the need for timely abuse
liability data and the need to determine
the most efficient tests to provide the
data necessary to make permanent
scheduling decisions. During the oneyear temporary scheduling period, DEA
must acquire sufficient data to make a
determination as to whether the
emergency scheduled substance should
remain under the CSA. Often the
substances have never been studied nor
are they available for study. DEA, as
soon as possible after identifying a
newly abused substance, provides for
the synthesis of this substance for
analytical reference standards and
biological testing. Only then can the
appropriate pharmacological and abuse
liability tests be conducted.
In an effort to assess the addiction
liability of these compounds, DEA
contracted studies of each of the
temporarily scheduled fentanyl
compounds at the University of
Michigan Medical School in Ann Arbor
and at the Medical College of Virginia
in Richmond. The studies indicated that
while most of the fentanyl compounds
had abuse liability profiles that
warranted control, two of these
temporarily scheduled compounds
(benzylfentanyl and thenylfentanyl) did
not have an addiction-forming or
addiction-sustaining liability similar to
morphine.
Based on the results of these studies,
on November 28, 1986, the DEA
extended the temporary scheduling of
six of these substances in schedule I.
However, benzylfentanyl and
thenylfentanyl were specifically omitted
from this extension (and any future
permanent control) because the
pharmacological and biological testing
of the substances, which included
assessment of morphine-like activity,
addiction liability, and analgesic effect,
indicated that the compounds were both
essentially inactive, with no evidence of
abuse potential.
Both of these substances were
temporarily controlled because they
were initially found in street samples
with other fentanyl analogues and were
most likely unreacted intermediates in
the synthesis of the target fentanyl
analogues. The DEA, having concluded
that these two drugs lacked morphinelike addictive properties, allowed the
temporary regulation of benzylfentanyl
and thenylfentanyl to expire on
November 29, 1986. Therefore, these
two substances were no longer regulated
as controlled substances upon that date.
In contrast, however, DEA chose to
extend temporary control of the other
four fentanyl compounds in a Final Rule
published November 26, 1986 (51 FR
42834) and permanently controlled
them in a Final Rule published May 29,
1987 (52 FR 20070).
Action of This Rulemaking
After the temporary listing of
benzylfentanyl and thenylfentanyl
expired in November of 1986, these
compounds were no longer controlled
under the CSA. However, DEA never
deleted 21 CFR 1308.11(g)(1) and (g)(2)
that reference the listing of these
compounds temporarily in schedule I.
This rulemaking hereby corrects the
CFR to delete 21 CFR 1308.11(g)(1) and
(g)(2) which previously stated:
(1) N-[1-benzyl-4-piperidyl]-N-phenylpropanamide (benzylfentanyl), its optical isomers, salts and salts of isomers ...........................
(2) N-[1-(2-thienyl)methyl-4-piperidyl]-N-phenylpropanamide (thenylfentanyl), its optical isomers, salts and salts of isomers ..........
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9834
Federal Register / Vol. 75, No. 124 / Tuesday, June 29, 2010 / Rules and Regulations
This action therefore corrects part
1308 to remove any reference to control
of benzylfentanyl and thenylfentanyl in
schedule I.
Regulatory Certifications
Administrative Procedure Act (5 U.S.C.
553)
An agency may find good cause to
exempt a rule from certain provisions of
the Administrative Procedure Act (5
U.S.C. 553), including notice of
proposed rulemaking and the
opportunity for public comment, if it is
determined to be unnecessary,
impracticable, or contrary to the public
interest. The temporary placement of
benzylfentanyl and thenylfentanyl in
Schedule I expired on November 29,
1986. The substances were never
scheduled and should have been
removed from Title 21 of the Code of
Federal Regulations, part 1308. This
Final Rule corrects this by removing
benzylfentanyl and thenylfentanyl from
the listing of controlled substances in
schedule I. As this Final Rule makes a
technical correction by removing
benzylfentanyl and thenylfentanyl from
the Code of Federal Regulations, DEA
finds it unnecessary and impracticable
to permit public notice and comment.
Therefore, DEA is publishing this
document as a final rule. Further, as the
removal of these substances prevents
confusion about the scheduling of these
substances, DEA finds there is good
cause to make this final rule effective
immediately upon publication.
wwoods2 on DSK1DXX6B1PROD with RULES
Regulatory Flexibility Act
The Deputy Administrator hereby
certifies that this rulemaking has been
drafted in accordance with the
Regulatory Flexibility Act (5 U.S.C.
601–612), and by approving it certifies
that this regulation will not have a
significant economic impact upon a
substantial number of small entities.
This action removes the substances
benzylfentanyl and thenylfentanyl from
the schedules of controlled substances.
These substances were temporarily
scheduled in 1985 under the emergency
scheduling provisions (21 U.S.C. 811, 21
CFR 1308.11(g)) and that temporary
scheduling expired on November 29,
1986; however, the substances were
never removed from the listing.
Executive Order 12866
The Deputy Administrator certifies
that this rulemaking has been drafted in
accordance with the principles in
Executive Order 12866 § 1(b). It has
been determined that this is not ‘‘a
significant regulatory action.’’ Therefore,
this action has not been reviewed by the
Office of Management and Budget.
VerDate Mar<15>2010
15:06 Jun 28, 2010
Jkt 220001
Executive Order 12988
This regulation meets the applicable
standards set forth in Sections 3(a) and
3(b)(2) of Executive Order 12988 Civil
Justice Reform.
Executive Order 13132
This rulemaking 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 are 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 cost 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 1308
Administrative practice and
procedure, Drug traffic control,
Reporting and recordkeeping
requirements.
■ For the reasons set out above, 21 CFR
part 1308 is amended as follows:
PART 1308—SCHEDULES OF
CONTROLLED SUBSTANCES
1. The authority citation for part 1308
continues to read as follows:
■
Authority: 21 U.S.C. 811, 812, 871(b)
unless otherwise noted.
2. Section 1308.11 is amended by
revising paragraph (g) to read as follows:
■
§ 1308.11
Schedule I.
*
*
*
*
*
(g) Temporary listing of substances
subject to emergency scheduling. Any
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37301
material, compound, mixture or
preparation which contains any
quantity of the following substances:
(1) [Reserved.]
(2) [Reserved.]
Dated: June 19, 2010.
Michele M. Leonhart,
Deputy Administrator.
[FR Doc. 2010–15529 Filed 6–28–10; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
21 CFR Part 1310
[Docket No. DEA–222F]
RIN 1117–AA64
Exempt Chemical Mixtures Containing
Gamma-Butyrolactone
AGENCY: Drug Enforcement
Administration (DEA), Justice.
ACTION: Final rule.
SUMMARY: This rulemaking finalizes a
November 12, 2008, Notice of Proposed
Rulemaking in which DEA proposed
that chemical mixtures that are 70
percent or less gamma-butyrolactone
(GBL), by weight or volume, be
automatically exempt from regulatory
controls under the Controlled
Substances Act (CSA). DEA is seeking
through this rulemaking to exempt only
those chemical mixtures that do not
represent a significant risk of diversion.
This regulation makes GBL chemical
mixtures, in concentrations greater than
70 percent, subject to List I chemical
regulatory requirements of the CSA,
except if exempted through an existing
categorical exemption. DEA is taking
this action because there is a serious
threat to the public safety associated
with the ease by which GBL is
chemically converted to the schedule I
controlled substance gammahydroxybutyric acid (GHB).
DEA recognizes that concentration
criteria alone cannot identify all
mixtures that warrant exemption. As a
result, DEA regulations provide for an
application process by which
manufacturers may obtain exemptions
from CSA regulatory controls for those
GBL chemical mixtures that are not
automatically exempt under the
concentration criteria.
DATES: This rulemaking becomes
effective July 29, 2010. Persons seeking
registration must apply on or before
July 29, 2010 to continue their business
pending final action by DEA on their
application.
E:\FR\FM\29JNR1.SGM
29JNR1
Agencies
[Federal Register Volume 75, Number 124 (Tuesday, June 29, 2010)]
[Rules and Regulations]
[Pages 37300-37301]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-15529]
[[Page 37300]]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
21 CFR Part 1308
[Docket No. DEA-313F]
RIN 1117-AB26
Correction of Code of Federal Regulations: Removal of Temporary
Listing of Benzylfentanyl and Thenylfentanyl as Controlled Substances
AGENCY: Drug Enforcement Administration (DEA), Department of Justice
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This rulemaking corrects Title 21 Code of Federal Regulations
(CFR) by deleting regulations which list the substances benzylfentanyl
and thenylfentanyl as being temporarily subject to schedule I controls
under the emergency scheduling provisions of the Controlled Substances
Act (CSA). The temporary scheduling of benzylfentanyl and
thenylfentanyl expired on November 29, 1986. DEA determined that these
compounds were both essentially inactive, with no evidence of abuse
potential. As such, these compounds are no longer schedule I controlled
substances and all references to these compounds are being deleted from
DEA regulations.
DATES: This rulemaking becomes effective June 29, 2010.
FOR FURTHER INFORMATION CONTACT: Christine A. Sannerud, PhD, Chief,
Drug and Chemical Evaluation Section, Office of Diversion Control, Drug
Enforcement Administration, 8701 Morrissette Drive, Springfield, VA
22152 at (202) 307-7183.
SUPPLEMENTARY INFORMATION: The CSA was amended by the Comprehensive
Crime Control Act of 1984 (Pub. L.98-473) which became effective on
October 12, 1984. This Act included a provision (21 U.S.C. 811(h))
which allows the DEA Administrator to place a substance, on a temporary
basis, into schedule I when necessary to avoid an imminent hazard to
the public safety. This emergency scheduling authority permits
scheduling a substance that is not currently controlled, is being
abused, and is a risk to the public health while the formal rulemaking
procedures (21 U.S.C. 811) described in the CSA are being conducted. A
temporary scheduling order may be issued for one year with a possible
extension of up to six months if formal scheduling procedures have been
initiated. The proposal and order are published in the Federal Register
as are the proposals and orders for formal scheduling. The emergency
scheduling authority was given to DEA in an effort to streamline the
scheduling process in response to the growing problem of controlled
substance analogues (``designer drugs'').
On October 29, 1985, DEA published a Final Rule (50 FR 43698) which
temporarily placed Acetyl-alpha-methylfentanyl, Alpha-
methylthiofentanyl, Beta-hydroxyfentanyl, Beta-hydroxy-3-
methylfentanyl, 3-Methylthiofentanyl, Thiofentanyl, Benzylfentanyl and
Thenylfentanyl into schedule I of the CSA. This control action became
effective on November 29, 1985.
These substances were emergency scheduled based on their appearance
in the illicit market, their similarity in chemical structure to that
of controlled substances, and the likelihood that they would produce
pharmacological effects similar to those of prototypic schedule I or II
substances. Often there is no biological data available prior to the
emergency control of illicitly produced and abused substances.
Therefore, information derived from structure-activity relationship
considerations plays an important role in emergency scheduling. To keep
an emergency scheduled substance in schedule I, DEA must initiate
traditional scheduling procedures (21 U.S.C. 811) for that substance
during the one year period in which it is emergency controlled and
complete the action before the expiration of 18 months. The time
limitations of emergency scheduling underscore the need for timely
abuse liability data and the need to determine the most efficient tests
to provide the data necessary to make permanent scheduling decisions.
During the one-year temporary scheduling period, DEA must acquire
sufficient data to make a determination as to whether the emergency
scheduled substance should remain under the CSA. Often the substances
have never been studied nor are they available for study. DEA, as soon
as possible after identifying a newly abused substance, provides for
the synthesis of this substance for analytical reference standards and
biological testing. Only then can the appropriate pharmacological and
abuse liability tests be conducted.
In an effort to assess the addiction liability of these compounds,
DEA contracted studies of each of the temporarily scheduled fentanyl
compounds at the University of Michigan Medical School in Ann Arbor and
at the Medical College of Virginia in Richmond. The studies indicated
that while most of the fentanyl compounds had abuse liability profiles
that warranted control, two of these temporarily scheduled compounds
(benzylfentanyl and thenylfentanyl) did not have an addiction-forming
or addiction-sustaining liability similar to morphine.
Based on the results of these studies, on November 28, 1986, the
DEA extended the temporary scheduling of six of these substances in
schedule I. However, benzylfentanyl and thenylfentanyl were
specifically omitted from this extension (and any future permanent
control) because the pharmacological and biological testing of the
substances, which included assessment of morphine-like activity,
addiction liability, and analgesic effect, indicated that the compounds
were both essentially inactive, with no evidence of abuse potential.
Both of these substances were temporarily controlled because they
were initially found in street samples with other fentanyl analogues
and were most likely unreacted intermediates in the synthesis of the
target fentanyl analogues. The DEA, having concluded that these two
drugs lacked morphine-like addictive properties, allowed the temporary
regulation of benzylfentanyl and thenylfentanyl to expire on November
29, 1986. Therefore, these two substances were no longer regulated as
controlled substances upon that date. In contrast, however, DEA chose
to extend temporary control of the other four fentanyl compounds in a
Final Rule published November 26, 1986 (51 FR 42834) and permanently
controlled them in a Final Rule published May 29, 1987 (52 FR 20070).
Action of This Rulemaking
After the temporary listing of benzylfentanyl and thenylfentanyl
expired in November of 1986, these compounds were no longer controlled
under the CSA. However, DEA never deleted 21 CFR 1308.11(g)(1) and
(g)(2) that reference the listing of these compounds temporarily in
schedule I. This rulemaking hereby corrects the CFR to delete 21 CFR
1308.11(g)(1) and (g)(2) which previously stated:
(1) N-[1-benzyl-4-piperidyl]-N-phenylpropanamide 9818
(benzylfentanyl), its optical isomers, salts and salts of
isomers.......................................................
(2) N-[1-(2-thienyl)methyl-4-piperidyl]-N-phenylpropanamide 9834
(thenylfentanyl), its optical isomers, salts and salts of
isomers.......................................................
[[Page 37301]]
This action therefore corrects part 1308 to remove any reference to
control of benzylfentanyl and thenylfentanyl in schedule I.
Regulatory Certifications
Administrative Procedure Act (5 U.S.C. 553)
An agency may find good cause to exempt a rule from certain
provisions of the Administrative Procedure Act (5 U.S.C. 553),
including notice of proposed rulemaking and the opportunity for public
comment, if it is determined to be unnecessary, impracticable, or
contrary to the public interest. The temporary placement of
benzylfentanyl and thenylfentanyl in Schedule I expired on November 29,
1986. The substances were never scheduled and should have been removed
from Title 21 of the Code of Federal Regulations, part 1308. This Final
Rule corrects this by removing benzylfentanyl and thenylfentanyl from
the listing of controlled substances in schedule I. As this Final Rule
makes a technical correction by removing benzylfentanyl and
thenylfentanyl from the Code of Federal Regulations, DEA finds it
unnecessary and impracticable to permit public notice and comment.
Therefore, DEA is publishing this document as a final rule. Further, as
the removal of these substances prevents confusion about the scheduling
of these substances, DEA finds there is good cause to make this final
rule effective immediately upon publication.
Regulatory Flexibility Act
The Deputy Administrator hereby certifies that this rulemaking has
been drafted in accordance with the Regulatory Flexibility Act (5
U.S.C. 601-612), and by approving it certifies that this regulation
will not have a significant economic impact upon a substantial number
of small entities. This action removes the substances benzylfentanyl
and thenylfentanyl from the schedules of controlled substances. These
substances were temporarily scheduled in 1985 under the emergency
scheduling provisions (21 U.S.C. 811, 21 CFR 1308.11(g)) and that
temporary scheduling expired on November 29, 1986; however, the
substances were never removed from the listing.
Executive Order 12866
The Deputy Administrator certifies that this rulemaking has been
drafted in accordance with the principles in Executive Order 12866
Sec. 1(b). It has been determined that this is not ``a significant
regulatory action.'' Therefore, this action has not been reviewed by
the Office of Management and Budget.
Executive Order 12988
This regulation meets the applicable standards set forth in
Sections 3(a) and 3(b)(2) of Executive Order 12988 Civil Justice
Reform.
Executive Order 13132
This rulemaking 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 are 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 cost
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 1308
Administrative practice and procedure, Drug traffic control,
Reporting and recordkeeping requirements.
0
For the reasons set out above, 21 CFR part 1308 is amended as follows:
PART 1308--SCHEDULES OF CONTROLLED SUBSTANCES
0
1. The authority citation for part 1308 continues to read as follows:
Authority: 21 U.S.C. 811, 812, 871(b) unless otherwise noted.
0
2. Section 1308.11 is amended by revising paragraph (g) to read as
follows:
Sec. 1308.11 Schedule I.
* * * * *
(g) Temporary listing of substances subject to emergency
scheduling. Any material, compound, mixture or preparation which
contains any quantity of the following substances:
(1) [Reserved.]
(2) [Reserved.]
Dated: June 19, 2010.
Michele M. Leonhart,
Deputy Administrator.
[FR Doc. 2010-15529 Filed 6-28-10; 8:45 am]
BILLING CODE 4410-09-P