Quotas - 2012
[Federal Register Volume 77, Number 129 (Thursday, July 5, 2012)]
[Notices]
[Pages 39737-39741]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-16396]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-363]
Controlled Substances: Proposed Adjustment to the Aggregate
Production Quotas for 2012
AGENCY: Drug Enforcement Administration (DEA), Department of Justice.
ACTION: Notice with request for comments.
SUMMARY: This notice proposes to adjust the 2012 aggregate production
quotas for several controlled substances in schedules I and II of the
Controlled Substances Act (CSA).
DATES: Electronic comments must be submitted and written comments must
be postmarked on or before August 6, 2012. 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-363" on all electronic and written correspondence.
DEA encourages all comments be submitted electronically through http://www.regulations.gov using the electronic comment form provided on that
site. An electronic copy of this document is also available at the
http://www.regulations.gov Web site for easy reference. Paper comments
that duplicate the electronic submission are not necessary as all
comments submitted to 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: John W. Partridge, Chief, Liaison and
Policy Section, Drug Enforcement Administration, 8701 Morrissette
Drive, Springfield, VA 22152, Telephone: (202) 307-4654.
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 http://www.regulations.gov and in the DEA's public docket. Such information
includes personal identifying
[[Page 39738]]
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 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 CONTACT paragraph.
Background
Section 306 of the CSA (21 U.S.C. 826) requires that the Attorney
General establish aggregate production quotas for each basic class of
controlled substance listed in schedules I and II. This responsibility
has been delegated to the Administrator of the DEA by 28 CFR 0.100. The
Administrator, in turn, has redelegated this function to the Deputy
Administrator, pursuant to 28 CFR 0.104. The 2012 established aggregate
production quotas for controlled substances in schedules I and II were
published in the Federal Register (76 FR 78044) on December 15, 2011.
That notice stipulated that, as provided for in 21 CFR 1303.13, all
aggregate production quotas are subject to adjustment.
Analysis for Proposed Revised 2012 Aggregate Production Quotas
DEA now proposes to adjust the established 2012 aggregate
production quotas for some schedule I and II controlled substances. In
proposing the adjustment, DEA has taken into account the criteria that
DEA is required to consider in accordance with 21 CFR 1303.13. DEA
proposes the adjustment of the aggregate production quotas for basic
classes of schedule I and II controlled substances by considering (1)
Changes in demand for the class, changes in the national rate of net
disposal for the class, and changes in the rate of net disposal by the
registrants holding individual manufacturing quotas for the class; (2)
whether any increased demand or changes in the national and/or
individual rates of net disposal are temporary, short term, or long
term; (3) whether any increased demand can be met through existing
inventories, increased individual manufacturing quotas, or increased
importation without increasing the aggregate production quota; (4)
whether any decreased demand will result in excessive inventory
accumulation by all persons registered to handle the class; and (5)
other factors affecting the medical, scientific, research, and
industrial needs of the United States and lawful export requirements,
as the Administrator finds relevant.
In determining whether to propose adjustments to the 2012 aggregate
production quotas, DEA considered updated information obtained from
2011 year-end inventories, 2011 disposition data submitted by quota
applicants, estimates of the medical needs of the United States,
product development, and other information made available to DEA after
the initial aggregate production quotas had been established. The
Deputy Administrator, therefore, proposes to adjust the 2012 aggregate
production quotas for some schedule I and II controlled substances,
expressed in grams of anhydrous acid or base, as follows:
| Basic class—Schedule I |
Previously
established
2012 quotas |
Proposed
adjusted 2012
quotas |
| 1-[1-(2-Thienyl)cyclohexyl]piperidine |
0 g |
5 g |
| 1-[2-(4-Morpholinyl)ethyl]-3-(1-naphthoyl)indole (JWH-200) |
45 g |
No Change |
| 1-Butyl-3-(1-naphthoyl)indole (JWH-073) |
45 g |
No Change |
| 1-Methyl-4-phenyl-4-propionoxypiperidine |
2 g |
No Change |
| 1-Pentyl-3-(1-naphthoyl)indole (JWH-018) |
45 g |
No Change |
| 2,5-Dimethoxyamphetamine |
2 g |
12 g |
| 2,5-Dimethoxy-4-ethylamphetamine (DOET) |
2 g |
12 g |
| 2,5-Dimethoxy-4-n-propylthiophenethylamine |
2 g |
12 g |
| 3-Methylfentanyl |
2 g |
No Change |
| 3-Methylthiofentanyl |
2 g |
No Change |
| 3,4-Methylenedioxyamphetamine (MDA) |
22 g |
30 g |
| 3,4-Methylenedioxy-N-methylcathinone (methylone) |
8 g |
12 g |
| 3,4-Methylenedioxy-N-ethylamphetamine (MDEA) |
15 g |
24 g |
| 3,4-Methylenedioxymethamphetamine (MDMA) |
22 g |
30 g |
| 3,4-Methylenedioxypyrovalerone (MDPV) |
8 g |
12 g |
| 3,4,5-Trimethoxyamphetamine |
2 g |
12 g |
| 4-Bromo-2,5-dimethoxyamphetamine (DOB) |
2 g |
12 g |
| 4-Bromo-2,5-dimethoxyphenethylamine (2-CB) |
2 g |
12 g |
| 4-Methoxyamphetamine |
77 g |
88 g |
| 4-Methylaminorex |
2 g |
12 g |
| 4-Methyl-2,5-dimethoxyamphetamine (DOM) |
2 g |
12 g |
| 4-Methyl-N-methylcathinone (mephedrone) |
8 g |
12 g |
| 5-(1,1-Dimethylheptyl)-2-[(1R,3S)-3-hydroxycyclohexyl]-phenol |
68 g |
No Change |
| 5-(1,1-Dimethyloctyl)-2-[(1R,3S)-3-hydroxycyclohexyl]-phenol |
53 g |
No Change |
| 5-Methoxy-3,4-methylenedioxyamphetamine |
2 g |
12 g |
| 5-Methoxy-N,N-diisopropyltryptamine |
2 g |
12 g |
| Acetyl-alpha-methylfentanyl |
2 g |
No Change |
| Acetyldihydrocodeine |
2 g |
No Change |
| Acetylmethadol |
2 g |
No Change |
| Allylprodine |
2 g |
No Change |
| Alphacetylmethadol |
2 g |
No Change |
| Alpha-ethyltryptamine |
2 g |
12 g |
| Alphameprodine |
2 g |
No Change |
| Alphamethadol |
2 g |
No Change |
| Alpha-methylfentanyl |
2 g |
No Change |
| Alpha-methylthiofentanyl |
2 g |
No Change |
| Alpha-methyltryptamine (AMT) |
2 g |
12 g |
| Aminorex |
2 g |
12 g |
| Benzylmorphine |
2 g |
No Change |
| Betacetylmethadol |
2 g |
No Change |
| Beta-hydroxy-3-methylfentanyl |
2 g |
No Change |
| Beta-hydroxyfentanyl |
2 g |
No Change |
| Betameprodine |
2 g |
No Change |
| Betamethadol |
2 g |
No Change |
| Betaprodine |
2 g |
No Change |
| Bufotenine |
3 g |
No Change |
| Cathinone |
4 g |
12 g |
| Codeine-N-oxide |
602 g |
No Change |
| Diethyltryptamine |
2 g |
12 g |
| Difenoxin |
50 g |
No Change |
| Dihydromorphine |
3,608,000 g |
No Change |
| Dimethyltryptamine |
7 g |
18 g |
| Gamma-hydroxybutyric acid |
47,000,000 g |
No Change |
| Heroin |
20 g |
No Change |
| Hydromorphinol |
54 g |
No Change |
| Hydroxypethidine |
2 g |
No Change |
| Ibogaine |
5 g |
No Change |
| Lysergic acid diethylamide (LSD) |
16 g |
No Change |
| Marihuana |
21,000 g |
No Change |
| Mescaline |
5 g |
13 g |
| Methaqualone |
10 g |
No Change |
| Methcathinone |
4 g |
12 g |
| Methyldihydromorphine |
2 g |
No Change |
| Morphine-N-oxide |
655 g |
No Change |
| N-Benzylpiperazine |
2 g |
12 g |
| N,N-Dimethylamphetamine |
2 g |
12 g |
| N-Ethylamphetamine |
2 g |
12 g |
| N-Hydroxy-3,4-methylenedioxyamphetamine |
2 g |
12 g |
| Noracymethadol |
2 g |
No Change |
| Norlevorphanol |
52 g |
No Change |
| Normethadone |
2 g |
No Change |
| Normorphine |
18 g |
No Change |
| Para-fluorofentanyl |
2 g |
No Change |
| Phenomorphan |
2 g |
No Change |
| Pholcodine |
2 g |
No Change |
| Properidine |
2 g |
No Change |
| Psilocybin |
2 g |
No Change |
| Psilocyn |
2 g |
No Change |
| Tetrahydrocannabinols |
393,000 g |
No Change |
| Thiofentanyl |
2 g |
No Change |
| Tilidine |
10 g |
No Change |
| Trimeperidine |
2 g |
No Change |
[[Page 39739]]
| Basic class—Schedule II |
Previously
established
2012 quotas |
Proposed
adjusted 2012
quotas |
| 1-Phenylcyclohexylamine |
2 g |
No Change |
| 1-Piperdinocyclohexanecarbonitrile |
2 g |
27 g |
| 4-Anilino-N-phenethyl-4-piperidine (ANPP) |
1,800,000 g |
No Change |
| Alfentanil |
15,000 g |
19,550 g |
| Alphaprodine |
2 g |
No Change |
| Amobarbital |
40,007 g |
No Change |
| Amphetamine (for conversion) |
8,500,000 g |
|
| Amphetamine (for sale) * |
25,300,000 g |
33,400,000 g |
| * DEA has determined that the revised total quantity to provide for the estimated medical, scientific, research, and industrial needs of the United States, lawful export requirements, and the establishment and maintenance of reserve stock is 29,400,000 g. DEA has further determined that an additional 4,000,000 g is necessary to provide for future research and development needs and unexpected emergencies that could affect market availability. |
| Carfentanil |
0 g |
5 g |
| Cocaine |
216,000 g |
No Change |
| Codeine (for conversion) |
65,000,000 g |
No Change |
| Codeine (for sale) |
39,605,000 g |
No Change |
| Dextropropoxyphene |
7 g |
No Change |
| Dihydrocodeine |
400,000 g |
No Change |
| Diphenoxylate |
900,000 g |
No Change |
| Ecgonine |
83,000 g |
No Change |
| Ethylmorphine |
2 g |
No Change |
| Fentanyl |
1,428,000 g |
No Change |
| Glutethimide |
2 g |
No Change |
| Hydrocodone (for sale) |
59,000,000 g |
63,000,000 g |
| Hydromorphone |
3,455,000 g |
3,628,000 g |
| Isomethadone |
4 g |
No Change |
| Levo-alphacetylmethadol (LAAM) |
3 g |
No Change |
| Levomethorphan |
5 g |
No Change |
| Levorphanol |
3,600 g |
No Change |
| Lisdexamfetamine |
12,000,000 g |
No Change |
| Meperidine |
5,500,000 g |
No Change |
| Meperidine Intermediate-A |
5 g |
No Change |
| Meperidine Intermediate-B |
9 g |
No Change |
| Meperidine Intermediate-C |
5 g |
No Change |
| Metazocine |
5 g |
No Change |
| Methadone (for sale) |
20,000,000 g |
No Change |
| Methadone Intermediate |
26,000,000 g |
No Change |
| Methamphetamine |
3,130,000 g |
No Change |
| [750,000 grams of levo-desoxyephedrine for use in a non-controlled, non-prescription product; 2,331,000 grams for methamphetamine mostly for conversion to a schedule III product; and 49,000 grams for methamphetamine (for sale)] |
| Methylphenidate |
56,000,000 g |
No Change |
| Morphine (for conversion) |
83,000,000 g |
No Change |
| Morphine (for sale) |
39,000,000 g |
No Change |
| Nabilone |
20,502 g |
No Change |
| Noroxymorphone (for conversion) |
7,200,000 g |
No Change |
| Noroxymorphone (for sale) |
401,000 g |
1,981,000 g |
| Opium (powder) |
63,000 g |
73,000 g |
| Opium (tincture) |
1,000,000 g |
No Change |
| Oripavine |
9,800,000 g |
15,300,000 g |
| Oxycodone (for conversion) |
5,600,000 g |
No Change |
| Oxycodone (for sale) |
98,000,000 g |
98,700,000 g |
| Oxymorphone (for conversion) |
12,800,000 g |
No Change |
| Oxymorphone (for sale) |
5,500,000 g |
No Change |
| Pentobarbital |
34,000,000 g |
No Change |
| Phenazocine |
5 g |
No Change |
| Phencyclidine |
24 g |
No Change |
| Phenmetrazine |
2 g |
No Change |
| Phenylacetone |
16,000,000 g |
No Change |
| Racemethorphan |
2 g |
No Change |
| Remifentanil |
2,500 g |
No Change |
| Secobarbital |
336,002 g |
No Change |
| Sufentanil |
5,000 g |
No Change |
| Tapentadol |
5,400,000 g |
No Change |
| Thebaine |
116,000,000 g |
No Change |
[[Page 39740]]
Aggregate production quotas for all other schedule I and II
controlled substances included in 21 CFR 1308.11 and 1308.12 remain at
zero. Pursuant to 21 CFR part 1303, the Deputy Administrator may adjust
the 2012 aggregate production quotas and individual manufacturing
quotas allocated for the year.
Comments
Pursuant to 21 CFR 1303.11 and 1303.13, any interested person may
submit written comments on or objections to these proposed
determinations. Based on comments received in response to this Notice,
the Deputy Administrator may hold a public hearing on one or more
issues raised. In the event the Deputy Administrator decides in his
sole discretion to hold such a hearing, the Deputy Administrator will
publish a notice of any such hearing in the Federal Register. After
consideration of any comments and after a hearing, if one is held, the
Deputy Administrator will publish in the Federal Register a Final
[[Page 39741]]
Order determining any adjustment of the aggregate production quota.
Dated: June 28, 2012.
Michele M. Leonhart,
Administrator.
[FR Doc. 2012-16396 Filed 7-3-12; 8:45 am]
BILLING CODE 4410-09-P
NOTICE: This is an unofficial version. An official version of this publication may be obtained
directly from the Government Printing Office (GPO). |
