Establishment of a New Drug Code for Marihuana Extract, 39039-39041 [2011-16800]
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Federal Register / Vol. 76, No. 128 / Tuesday, July 5, 2011 / Proposed Rules
keep them operationally current. It,
therefore, (1) Is not a ‘‘significant
regulatory action’’ under Executive
Order 12866; (2) is not a ‘‘significant
rule’’ under DOT Regulatory Policies
and Procedures (44 FR 11034; February
26, 1979); and (3) does not warrant
preparation of a Regulatory Evaluation
as the anticipated impact is so minimal.
Since this is a routine matter that will
only affect air traffic procedures and air
navigation, it is certified that this
proposed rule, when promulgated,
would not have a significant economic
impact on a substantial number of small
entities under the criteria of the
Regulatory Flexibility Act.
The FAA’s authority to issue rules
regarding aviation safety is found in
Title 49 of the United States Code.
Subtitle I, section 106 describes the
authority of the FAA Administrator.
Subtitle VII, Aviation Programs,
describes in more detail the scope of the
agency’s authority. This proposed
rulemaking is promulgated under the
authority described in subtitle VII, part,
A, subpart I, section 40103. Under that
section, the FAA is charged with
prescribing regulations to assign the use
of airspace necessary to ensure the
safety of aircraft and the efficient use of
airspace. This proposed regulation is
within the scope of that authority as it
would establish Class E airspace at
Keller Brothers Airport, Lebanon, PA.
Lists of Subjects in 14 CFR Part 71
Airspace, Incorporation by reference,
Navigation (air).
The Proposed Amendment
In consideration of the foregoing, the
Federal Aviation Administration
proposes to amend 14 CFR part 71 as
follows:
PART 71—DESIGNATION OF CLASS A,
B, C, D, AND E AIRSPACE AREAS; AIR
TRAFFIC SERVICE ROUTES; AND
REPORTING POINTS
1. The authority citation for part 71
continues to read as follows:
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Authority: 49 U.S.C. 106(g); 40103, 40113,
40120; E.O. 10854, 24 FR 9565, 3 CFR, 1959–
1963 Comp., p. 389.
§ 71.1
[Amended]
2. The incorporation by reference in
14 CFR 71.1 of Federal Aviation
Administration Order 7400.9U,
Airspace Designations and Reporting
Points, dated August 18, 2010, effective
September 15, 2010, is amended as
follows:
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Paragraph 6005 Class E airspace areas
extending upward from 700 feet or more
above the surface of the earth.
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*
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*
*
AEA PA E5 Lebanon, PA [New]
Keller Brothers Airport
(Lat. 40°917′30″ N., long. 76°19′43″ W.)
That airspace extending upward from 700
feet above the surface within a 10-mile radius
of the Keller Brothers Airport.
Issued in College Park, Georgia, on June 23,
2011.
Mark D. Ward,
Manager, Operations Support Group, Eastern
Service Center, Air Traffic Organization.
[FR Doc. 2011–16660 Filed 7–1–11; 8:45 am]
BILLING CODE 4910–13–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
21 CFR Part 1308
[Docket No. DEA–342P]
RIN 1117–AB33
Establishment of a New Drug Code for
Marihuana Extract
Drug Enforcement
Administration, Department of Justice.
ACTION: Notice of proposed rulemaking.
AGENCY:
The Drug Enforcement
Administration (DEA) is proposing to
create a new Administration Controlled
Substances Code Number (‘‘Code
Number’’ or ‘‘drug code’’) under 21 CFR
1308.11 for ‘‘Marihuana Extract.’’ This
Code Number will allow DEA and DEAregistered entities to track quantities of
this material separately from quantities
of marihuana. This in turn will aid in
complying with relevant treaty
provisions.
Under international drug control
treaties (administered by the United
Nations), some differences exist
between the regulatory controls
pertaining to marihuana extract versus
those for marihuana and
tetrahydrocannabinols. DEA has
established separate Code Numbers for
marihuana and for
tetrahydrocannabinols, but not for
marihuana extract. To better track these
materials and better comply with treaty
provisions, DEA is proposing to create
a separate Code Number for marihuana
extract under 21 CFR 1308.11(d)(36):
‘‘Marihuana Extract meaning extracts
that have been derived from any plant
of the genus cannabis and which
contain cannabinols and cannabidiols.’’
Such extracts of marihuana would
continue to be treated as schedule I
controlled substances.
SUMMARY:
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39039
Electronic comments must be
submitted and written comments must
be postmarked on or before September
6, 2011. Commenters should be aware
that the electronic Federal Docket
Management System will not accept
comments after midnight Eastern Time
on the last day of the comment period.
ADDRESSES: To ensure proper handling
of comments, please reference ‘‘Docket
No. DEA–342’’ on all electronic and
written correspondence. DEA
encourages all comments be submitted
electronically through https://
www.regulations.gov using the
electronic comment form provided on
that site. An electronic copy of this
document and supplemental
information to this proposed rule are
also available at the https://
www.regulations.gov Web site for easy
reference. Paper comments that
duplicate the electronic submission are
not necessary as all comments
submitted to https://www.regulations.gov
will be posted for public review and are
part of the official docket record. Should
you, however, wish to submit written
comments via regular or express mail,
they should be sent to the Drug
Enforcement Administration, Attention:
DEA Federal Register Representative/
ODL, 8701 Morrissette Drive,
Springfield, VA 22152.
FOR FURTHER INFORMATION CONTACT:
Imelda L. Paredes, Office of Diversion
Control, Drug Enforcement
Administration, 8701 Morrissette Drive,
Springfield, Virginia 22152; Telephone
(202) 307–7165.
SUPPLEMENTARY INFORMATION:
Posting of Public Comments: Please
note that all comments received are
considered part of the public record and
made available for public inspection
online at https://www.regulations.gov
and in the DEA’s public docket. Such
information includes personal
identifying information (such as your
name, address, etc.) voluntarily
submitted by the commenter.
If you want to submit personal
identifying information (such as your
name, address, etc.) as part of your
comment, but do not want it to be
posted online or made available in the
public docket, you must include the
phrase ‘‘PERSONAL IDENTIFYING
INFORMATION’’ in the first paragraph
of your comment. You must also place
all the personal identifying information
you do not want posted online or made
available in the public docket in the first
paragraph of your comment and identify
what information you want redacted.
If you want to submit confidential
business information as part of your
comment, but do not want it to be
DATES:
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05JYP1
39040
Federal Register / Vol. 76, No. 128 / Tuesday, July 5, 2011 / Proposed Rules
mstockstill on DSK4VPTVN1PROD with PROPOSALS
posted online or made available in the
public docket, you must include the
phrase ‘‘CONFIDENTIAL BUSINESS
INFORMATION’’ in the first paragraph
of your comment. You must also
prominently identify confidential
business information to be redacted
within the comment. If a comment has
so much confidential business
information that it cannot be effectively
redacted, all or part of that comment
may not be posted online or made
available in the public docket.
Personal identifying information and
confidential business information
identified and located as set forth above
will be redacted, and the comment, in
redacted form, will be posted online and
placed in the DEA’s public docket file.
Please note that the Freedom of
Information Act applies to all comments
received. If you wish to inspect the
agency’s public docket file in person by
appointment, please see the ‘‘For
Further Information’’ paragraph.
Background
As provided in 21 CFR 1308.03, each
controlled substance or basic class
thereof is assigned a four digit Code
Number that is used to track quantities
of the controlled substance imported
and exported to and from the United
States. Additionally, DEA uses these
Code Numbers in establishing aggregate
production quotas for basic classes of
controlled substances listed in
schedules I and II as required by 21
U.S.C. 826.
Consistent with the Controlled
Substances Act (CSA), the schedules
contained in the DEA regulations
include marihuana (drug code 7360) in
schedule I. 21 CFR 1308.11(d)(23). This
listing includes (unless specifically
excepted or unless listed in another
schedule) any material, compound,
mixture, or preparation, which contains
any quantity of the substance, or which
contains any of its salts, isomers, and
salts of isomers that are possible within
the specific chemical designation.
Because the definition of marihuana in
21 U.S.C. 802(16) includes both
derivatives and preparations of
marihuana, DEA until now has used
drug code 7360 for extracts of
marihuana as well. In this proposed
rule, DEA is proposing that the new
drug code 7350 be used for extracts of
marihuana.
Why a New Code Number Is Needed
The United Nations Conventions on
international drug control treat extracts
from the cannabis plant differently than
marihuana or tetrahydrocannabinols.
The creation of a new drug code in DEA
regulations for marihuana extracts will
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17:41 Jul 01, 2011
Jkt 223001
allow for more appropriate accounting
of such materials consistent with treaty
provisions.
The Single Convention on Narcotic
Drugs, 1961 (‘‘Single Convention’’) and
the 1971 Convention on Psychotropic
Substances (‘‘Psychotropic
Convention’’) provide for the
international control of marihuana
constituents. Many of the CSA’s
provisions were drafted to comply with
these Conventions. The CSA includes
schemes of drug scheduling and
procedures for adding, removing, and
transferring drugs among the schedules
that are similar, in some ways, to those
in the Single Convention. With respect
to those drugs that are subject to control
under the Single Convention, the CSA
mandates that DEA control such drugs
at least as strictly as required by the
Single Convention. 21 U.S.C. 811(d).
Somewhat similar to the CSA, the
Single Convention controls substances
through four schedules. However, under
the Single Convention, the drugs that
are subject to the most stringent controls
are in schedule IV. Another difference
between the CSA and the Single
Convention is that, under the latter, a
drug can be listed in more than one
schedule. Cannabis and cannabis resin
are listed in both schedule IV and
schedule I of the Single Convention.
Schedule I controls under the Single
Convention include requirements for
import and export authorization,
licensing of manufacturers/distributors,
recordkeeping requirements,
requirement for prescriptions for
medical use, annual estimate of needs,
quotas, annual statistical reporting, and
a requirement that use be limited to
medical and scientific purposes.
Schedule II of the Single Convention is
similar in controls to schedule I with a
few exceptions, and schedule III is less
restrictive. All substances listed in
schedule IV are also listed in schedule
I. The placing of a drug into both
schedule I and schedule IV therefore
imposes the most stringent controls
under the Single Convention. Although
cannabis and cannabis resin are listed in
Schedules I and IV of the Single
Convention, cannabis extracts are listed
only in Schedule I.
Proposed Actions
DEA therefore proposes to update 21
CFR 1308.11(d) to include new
subparagraph (36) which would create a
new Code Number in schedule I as
follows:
‘‘(36) Marihuana Extract ..............
7350
Meaning extracts that have been derived
from any plant of the genus cannabis and
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Fmt 4702
Sfmt 4702
which contain cannabinols and
cannabidiols.’’
The creation of a new drug code in
DEA regulations for marihuana extracts
would allow for more appropriate
accounting of such materials consistent
with treaty provisions. Such marihuana
extracts remain in schedule I. Firms
registered to handle marihuana (under
drug code 7360) that also handle
marihuana extracts, will need to apply
to add the new drug code 7350 to their
existing DEA registrations and procure
quotas specifically for drug code 7350
each year.
Regulatory Compliance Analyses
Regulatory Flexibility Act
In accordance with the Regulatory
Flexibility Act (5 U.S.C. 601–612), the
Administrator has reviewed this
regulation and by approving it certifies
that this regulation will not have a
significant economic impact upon a
substantial number of small entities.
This rule proposes the establishment of
a new drug code for marihuana extracts.
DEA already registers persons handling
marihuana extracts, but within another
already-established drug code. Thus,
persons who handle these marihuana
extracts have already met DEA’s
registration, security, and other
statutory and regulatory requirements.
The only direct effect to registrants who
handle marihuana extracts would be the
requirement to add the new drug code
to their registration once the code is
established.
Executive Orders 12866 and 13563
This regulation has been drafted and
reviewed in accordance with the
principles of Executive Orders 12866
and 13563. Although this rule is not a
‘‘significant regulatory action’’ under
Executive Order 12866 Section 3(f), it
was submitted to the Office of
Management and Budget (OMB) and
subsequently approved.
Executive Order 12988
This proposed regulation meets the
applicable standards set forth in
Sections 3(a) and 3(b)(2) of Executive
Order 12988 Civil Justice Reform to
eliminate ambiguity, minimize
litigation, establish clear legal standards
and reduce burden.
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
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Federal Register / Vol. 76, No. 128 / Tuesday, July 5, 2011 / Proposed Rules
implications warranting the application
of Executive Order 13132.
DEPARTMENT OF LABOR
Unfunded Mandates Reform Act of 1995
Occupational Safety and Health
Administration
This rule will not result in the
expenditure by state, local, and Tribal
governments, in the aggregate, or by the
private sector, of $136,000,000 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.
29 CFR Part 1910
RIN 1218–AC46
Infectious Diseases
Occupational Safety and Health
Administration (OSHA), Labor.
ACTION: Notice of stakeholder meetings.
AGENCY:
OSHA invites interested
parties to participate in informal
stakeholder meetings concerning
occupational exposure to infectious
This action does not impose a
diseases. OSHA plans to use the
collection of information requirement
information gathered at these meetings
under the Paperwork Reduction Act of
to explore the possible development of
1995, 44 U.S.C. 3501–3521.
a proposed rule to protect workers from
Executive Order 13175
occupational exposure to infectious
agents in settings, either where workers
This rule is not a policy that has
provide direct patient care or where
Tribal implications under Executive
Order 13175. It will not have substantial workers perform tasks other than direct
patient care that also have occupational
direct effects on one or more Indian
exposure. These other work tasks
Tribes, on the relationship between the
include: Providing patient support
Federal Government and Indian Tribes,
services (e.g., housekeeping, facility
or on the distribution of power and
maintenance); handling, transporting,
responsibilities between the Federal
receiving or processing infectious items
Government and Indian Tribes.
or wastes (e.g., transporting medical
specimens, disposing of medical waste);
List of Subjects in 21 CFR Part 1308
conducting autopsies or performing
Drug traffic control, Controlled
mortuary services; and performing tasks
substances.
in laboratories.
DATES: Dates and locations for the
For the reasons set out above, 21 CFR
stakeholder meetings are:
part 1308 is proposed to be amended as
July 29, 2011, 9 a.m.–noon in
follows:
Washington, DC.
July 29, 2011, 1:30 p.m.–4:30 p.m. in
PART 1308—SCHEDULES OF
Washington, DC.
CONTROLLED SUBSTANCES
The deadline for confirmed
1. The authority citation for part 1308 registration at the meeting is: July 22,
2011. However, if space remains after
continues to read as follows:
this deadline, OSHA may accept
Authority: 21 U.S.C. 811, 812, 871(b).
additional participants until the
meetings are full. Those who submit
2. Section 1308.11 is amended by
adding new paragraph (d)(36) to read as their registration after July 22, 2011 may
not receive confirmation of their
follows:
attendance from OSHA.
§ 1308.11 Schedule I.
ADDRESSES:
Registration: Submit your notice of
*
*
*
*
*
intent to participate in a stakeholder
(d) * * *
meeting through one of the methods
(36) Marihuana Extract ................
7350 below. Specify which meeting (morning
or afternoon) you would like to attend.
Meaning extracts that have been
Electronic: Register at: https://
derived from any plant of the genus
www2.ergweb.com/projects/
cannabis and which contain
conferences/osha/register-oshacannabinols and cannabidiols.
stakeholder.htm (follow the instructions
*
*
*
*
*
online).
Facsimile: Fax your request to: (781)
Dated: June 14, 2011.
674–7200, and label it ‘‘Attention:
Michele M. Leonhart,
OSHA Infectious Diseases Stakeholder
Administrator.
Meeting Registration.’’
[FR Doc. 2011–16800 Filed 7–1–11; 8:45 am]
Regular mail, express delivery, hand
(courier) delivery, and messenger
BILLING CODE 4410–09–P
SUMMARY:
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Paperwork Reduction Act of 1995
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17:41 Jul 01, 2011
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39041
service: Send your request to: OSHA
Infectious Diseases Stakeholder Meeting
Registration, Attention: Thomas Nerad,
OSHA, Room N–3718, 200 Constitution
Avenue, NW., Washington, DC 20210.
Meetings: The July 29, 2011 meetings
will be held in the Francis Perkins
Building, Room N–4437 at 200
Constitution Avenue, NW., Washington,
DC 20210.
FOR FURTHER INFORMATION CONTACT:
Information regarding this notice is
available from the following sources:
Press inquiries: Contact Frank
Meilinger, Acting Director, OSHA Office
of Communications, Room N–3647, U.S.
Department of Labor, 200 Constitution
Avenue, NW., Washington, DC 20210;
telephone: (202) 693–1999.
General and technical information:
Contact Andrew Levinson, Director,
Office of Biological Hazards, OSHA
Directorate of Standards and Guidance,
Room N–3718, U.S. Department of
Labor, 200 Constitution Avenue, NW.,
Washington, DC 20210; telephone: (202)
693–2048.
Copies of this Federal Register
notice: Electronic copies are available at
https://www.regulations.gov. This
Federal Register notice, as well as news
releases and other relevant information,
also are available on the OSHA Web
page at https://www.osha.gov.
SUPPLEMENTARY INFORMATION:
I. Background
On May 6, 2010, OSHA published a
Request for Information, entitled
‘‘Infectious Diseases’’ (Docket Number:
OSHA–2010–0003). The Agency was
interested in more accurately
characterizing the nature and extent of
occupationally-acquired infectious
diseases and the strategies that are
currently being used to mitigate the risk
of occupational exposure to infectious
agents. More than 200 comments were
received in response to the RFI. Based
upon these responses and an ongoing
review of current literature on this
subject, OSHA is considering what
action, if any, the Agency should take to
limit the spread of occupationallyacquired infectious diseases.
One action the Agency is considering
is the development of a program
standard to control workers’ exposure to
infectious agents in settings, either
where workers provide direct patient
care or where workers perform tasks
other than direct patient care which also
have occupational exposure. These
other tasks might include such tasks as:
Providing patient support services (e.g.,
housekeeping, food delivery, facility
maintenance); handling, transporting,
receiving or processing infectious items
E:\FR\FM\05JYP1.SGM
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Agencies
[Federal Register Volume 76, Number 128 (Tuesday, July 5, 2011)]
[Proposed Rules]
[Pages 39039-39041]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-16800]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
21 CFR Part 1308
[Docket No. DEA-342P]
RIN 1117-AB33
Establishment of a New Drug Code for Marihuana Extract
AGENCY: Drug Enforcement Administration, Department of Justice.
ACTION: Notice of proposed rulemaking.
-----------------------------------------------------------------------
SUMMARY: The Drug Enforcement Administration (DEA) is proposing to
create a new Administration Controlled Substances Code Number (``Code
Number'' or ``drug code'') under 21 CFR 1308.11 for ``Marihuana
Extract.'' This Code Number will allow DEA and DEA-registered entities
to track quantities of this material separately from quantities of
marihuana. This in turn will aid in complying with relevant treaty
provisions.
Under international drug control treaties (administered by the
United Nations), some differences exist between the regulatory controls
pertaining to marihuana extract versus those for marihuana and
tetrahydrocannabinols. DEA has established separate Code Numbers for
marihuana and for tetrahydrocannabinols, but not for marihuana extract.
To better track these materials and better comply with treaty
provisions, DEA is proposing to create a separate Code Number for
marihuana extract under 21 CFR 1308.11(d)(36): ``Marihuana Extract
meaning extracts that have been derived from any plant of the genus
cannabis and which contain cannabinols and cannabidiols.'' Such
extracts of marihuana would continue to be treated as schedule I
controlled substances.
DATES: Electronic comments must be submitted and written comments must
be postmarked on or before September 6, 2011. Commenters should be
aware that the electronic Federal Docket Management System will not
accept comments after midnight Eastern Time on the last day of the
comment period.
ADDRESSES: To ensure proper handling of comments, please reference
``Docket No. DEA-342'' on all electronic and written correspondence.
DEA encourages all comments be submitted electronically through https://www.regulations.gov using the electronic comment form provided on that
site. An electronic copy of this document and supplemental information
to this proposed rule are also available at the https://www.regulations.gov Web site for easy reference. Paper comments that
duplicate the electronic submission are not necessary as all comments
submitted to https://www.regulations.gov will be posted for public
review and are part of the official docket record. Should you, however,
wish to submit written comments via regular or express mail, they
should be sent to the Drug Enforcement Administration, Attention: DEA
Federal Register Representative/ODL, 8701 Morrissette Drive,
Springfield, VA 22152.
FOR FURTHER INFORMATION CONTACT: Imelda L. Paredes, Office of Diversion
Control, Drug Enforcement Administration, 8701 Morrissette Drive,
Springfield, Virginia 22152; Telephone (202) 307-7165.
SUPPLEMENTARY INFORMATION:
Posting of Public Comments: Please note that all comments received
are considered part of the public record and made available for public
inspection online at https://www.regulations.gov and in the DEA's public
docket. Such information includes personal identifying information
(such as your name, address, etc.) voluntarily submitted by the
commenter.
If you want to submit personal identifying information (such as
your name, address, etc.) as part of your comment, but do not want it
to be posted online or made available in the public docket, you must
include the phrase ``PERSONAL IDENTIFYING INFORMATION'' in the first
paragraph of your comment. You must also place all the personal
identifying information you do not want posted online or made available
in the public docket in the first paragraph of your comment and
identify what information you want redacted.
If you want to submit confidential business information as part of
your comment, but do not want it to be
[[Page 39040]]
posted online or made available in the public docket, you must include
the phrase ``CONFIDENTIAL BUSINESS INFORMATION'' in the first paragraph
of your comment. You must also prominently identify confidential
business information to be redacted within the comment. If a comment
has so much confidential business information that it cannot be
effectively redacted, all or part of that comment may not be posted
online or made available in the public docket.
Personal identifying information and confidential business
information identified and located as set forth above will be redacted,
and the comment, in redacted form, will be posted online and placed in
the DEA's public docket file. Please note that the Freedom of
Information Act applies to all comments received. If you wish to
inspect the agency's public docket file in person by appointment,
please see the ``For Further Information'' paragraph.
Background
As provided in 21 CFR 1308.03, each controlled substance or basic
class thereof is assigned a four digit Code Number that is used to
track quantities of the controlled substance imported and exported to
and from the United States. Additionally, DEA uses these Code Numbers
in establishing aggregate production quotas for basic classes of
controlled substances listed in schedules I and II as required by 21
U.S.C. 826.
Consistent with the Controlled Substances Act (CSA), the schedules
contained in the DEA regulations include marihuana (drug code 7360) in
schedule I. 21 CFR 1308.11(d)(23). This listing includes (unless
specifically excepted or unless listed in another schedule) any
material, compound, mixture, or preparation, which contains any
quantity of the substance, or which contains any of its salts, isomers,
and salts of isomers that are possible within the specific chemical
designation. Because the definition of marihuana in 21 U.S.C. 802(16)
includes both derivatives and preparations of marihuana, DEA until now
has used drug code 7360 for extracts of marihuana as well. In this
proposed rule, DEA is proposing that the new drug code 7350 be used for
extracts of marihuana.
Why a New Code Number Is Needed
The United Nations Conventions on international drug control treat
extracts from the cannabis plant differently than marihuana or
tetrahydrocannabinols. The creation of a new drug code in DEA
regulations for marihuana extracts will allow for more appropriate
accounting of such materials consistent with treaty provisions.
The Single Convention on Narcotic Drugs, 1961 (``Single
Convention'') and the 1971 Convention on Psychotropic Substances
(``Psychotropic Convention'') provide for the international control of
marihuana constituents. Many of the CSA's provisions were drafted to
comply with these Conventions. The CSA includes schemes of drug
scheduling and procedures for adding, removing, and transferring drugs
among the schedules that are similar, in some ways, to those in the
Single Convention. With respect to those drugs that are subject to
control under the Single Convention, the CSA mandates that DEA control
such drugs at least as strictly as required by the Single Convention.
21 U.S.C. 811(d).
Somewhat similar to the CSA, the Single Convention controls
substances through four schedules. However, under the Single
Convention, the drugs that are subject to the most stringent controls
are in schedule IV. Another difference between the CSA and the Single
Convention is that, under the latter, a drug can be listed in more than
one schedule. Cannabis and cannabis resin are listed in both schedule
IV and schedule I of the Single Convention. Schedule I controls under
the Single Convention include requirements for import and export
authorization, licensing of manufacturers/distributors, recordkeeping
requirements, requirement for prescriptions for medical use, annual
estimate of needs, quotas, annual statistical reporting, and a
requirement that use be limited to medical and scientific purposes.
Schedule II of the Single Convention is similar in controls to schedule
I with a few exceptions, and schedule III is less restrictive. All
substances listed in schedule IV are also listed in schedule I. The
placing of a drug into both schedule I and schedule IV therefore
imposes the most stringent controls under the Single Convention.
Although cannabis and cannabis resin are listed in Schedules I and IV
of the Single Convention, cannabis extracts are listed only in Schedule
I.
Proposed Actions
DEA therefore proposes to update 21 CFR 1308.11(d) to include new
subparagraph (36) which would create a new Code Number in schedule I as
follows:
``(36) Marihuana Extract..................................... 7350
Meaning extracts that have been derived from any plant of the
genus cannabis and which contain cannabinols and cannabidiols.''
The creation of a new drug code in DEA regulations for marihuana
extracts would allow for more appropriate accounting of such materials
consistent with treaty provisions. Such marihuana extracts remain in
schedule I. Firms registered to handle marihuana (under drug code 7360)
that also handle marihuana extracts, will need to apply to add the new
drug code 7350 to their existing DEA registrations and procure quotas
specifically for drug code 7350 each year.
Regulatory Compliance Analyses
Regulatory Flexibility Act
In accordance with the Regulatory Flexibility Act (5 U.S.C. 601-
612), the Administrator has reviewed this regulation and by approving
it certifies that this regulation will not have a significant economic
impact upon a substantial number of small entities. This rule proposes
the establishment of a new drug code for marihuana extracts. DEA
already registers persons handling marihuana extracts, but within
another already-established drug code. Thus, persons who handle these
marihuana extracts have already met DEA's registration, security, and
other statutory and regulatory requirements. The only direct effect to
registrants who handle marihuana extracts would be the requirement to
add the new drug code to their registration once the code is
established.
Executive Orders 12866 and 13563
This regulation has been drafted and reviewed in accordance with
the principles of Executive Orders 12866 and 13563. Although this rule
is not a ``significant regulatory action'' under Executive Order 12866
Section 3(f), it was submitted to the Office of Management and Budget
(OMB) and subsequently approved.
Executive Order 12988
This proposed regulation meets the applicable standards set forth
in Sections 3(a) and 3(b)(2) of Executive Order 12988 Civil Justice
Reform to eliminate ambiguity, minimize litigation, establish clear
legal standards and reduce burden.
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
[[Page 39041]]
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
$136,000,000 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.
Paperwork Reduction Act of 1995
This action does not impose a collection of information requirement
under the Paperwork Reduction Act of 1995, 44 U.S.C. 3501-3521.
Executive Order 13175
This rule is not a policy that has Tribal implications under
Executive Order 13175. It will not have substantial direct effects on
one or more Indian Tribes, on the relationship between the Federal
Government and Indian Tribes, or on the distribution of power and
responsibilities between the Federal Government and Indian Tribes.
List of Subjects in 21 CFR Part 1308
Drug traffic control, Controlled substances.
For the reasons set out above, 21 CFR part 1308 is proposed to be
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).
2. Section 1308.11 is amended by adding new paragraph (d)(36) to
read as follows:
Sec. 1308.11 Schedule I.
* * * * *
(d) * * *
(36) Marihuana Extract....................................... 7350
Meaning extracts that have been derived from any plant of the genus
cannabis and which contain cannabinols and cannabidiols.
* * * * *
Dated: June 14, 2011.
Michele M. Leonhart,
Administrator.
[FR Doc. 2011-16800 Filed 7-1-11; 8:45 am]
BILLING CODE 4410-09-P