Skip to Content

Notice

Controlled Substances: Established Initial Aggregate Production Quotas for 2003

Document Details

Information about this document as published in the Federal Register.

Published Document

This document has been published in the Federal Register. Use the PDF linked in the document sidebar for the official electronic format.

Start Preamble

AGENCY:

Drug Enforcement Administration (DEA), Justice.

ACTION:

Notice of aggregate production quotas for 2003.

SUMMARY:

This notice establishes initial 2003 aggregate production quotas for controlled substances in Schedules I and II of the Controlled Substances Act (CSA).

EFFECTIVE DATE:

December 19, 2002.

Start Further Info

FOR FURTHER INFORMATION CONTACT:

Frank L. Sapienza, Chief, Drug & Chemical Evaluation Section, Drug Enforcement Administration, Washington, D.C. 20537, Telephone: (202) 307-7183.

End Further Info End Preamble Start Supplemental Information

SUPPLEMENTARY INFORMATION:

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 Section 0.100 of Title 28 of the Code of Federal Regulations. The Administrator, in turn, has redelegated this function to the Deputy Administrator, pursuant to Section 0.104 of Title 28 of the Code of Federal Regulations.

The 2003 aggregate production quotas represent those quantities of controlled substances that may be produced in the United States in 2003 to provide adequate supplies of each substance for: the estimated medical, scientific, research and industrial needs of the United States; lawful export requirements; and the establishment and maintenance of reserve stocks (21 U.S.C. 826(a) and 21 CFR 1303.11). These quotas do not include imports of controlled substances for use in industrial processes.

On November 1, 2002, a notice of the proposed initial 2003 aggregate production quotas for certain controlled substances in Schedules I and II was published in the Federal Register (67 FR 66663). All interested persons were invited to comment on or object to these proposed aggregate production quotas on or before November 22, 2002.

Ten companies commented on a total of twenty Schedules I and II controlled substances within the published comment period. The companies commented that the proposed aggregate production quotas for amobarbital, amphetamine, codeine (for sale), codeine (for conversion), dextropropoxyphene, dihydrocodeine, fentanyl, glutethimide, hydrocodone (for sale), hydromorphone, methadone (for sale), methadone intermediate, methamphetamine (for conversion), methamphetamine (for sale), morphine (for conversion), noroxymorphone (for sale), opium, oxycodone (for sale), sufentanil and thebaine were insufficient to provide for the estimated medical, scientific, research and industrial needs of the United States, for export requirements and for the establishment and maintenance of reserve stocks. One company commented that the proposed aggregate production quota for methamphetamine (for sale) was adequate to provide for the estimated medical needs of the United States.

DEA has taken into consideration the above comments along with the relevant 2002 manufacturing quotas, current 2002 sales and inventories, 2003 export requirements and research and product development requirements, and Start Printed Page 77810additional and revised applications for 2003 manufacturing quotas. Based on this information, the DEA has adjusted the initial aggregate production quotas for amobarbital, codeine (for conversion), codeine-N-oxide, glutethimide, methadone (for sale), methadone intermediate, levo-desoxyephedrine, methamphetamine (for conversion), morphine-N-oxide, opium, and sufentanil to meet the legitimate needs of the United States.

Regarding amphetamine, codeine (for sale), dextropropoxyphene, dihydrocodeine, fentanyl, hydrocodone (for sale), hydromorphone, morphine (for conversion), noroxymorphone (for sale), oxycodone (for sale), and thebaine, the DEA has determined that the proposed initial 2003 aggregate production quotas are sufficient to meet the current 2003 estimated medical, scientific, research and industrial needs of the United States.

Pursuant to Section 1303 of Title 21 of the Code of Federal Regulations, the Deputy Administrator of the DEA will, in early 2003, adjust aggregate production quotas and individual manufacturing quotas allocated for the year based upon 2002 year-end inventory and actual 2002 disposition data supplied by quota recipients for each basic class of Schedules I and II controlled substance.

Therefore, under the authority vested in the Attorney General by Section 306 of the Controlled Substances Act of 1970 (21 U.S.C. 826), and delegated to the Administrator of the DEA by Section 0.100 of Title 28 of the Code of Federal Regulations, and redelegated to the Deputy Administrator pursuant to Section 0.104 of Title 28 of the Code of Federal Regulations, the Deputy Administrator hereby orders that the 2003 initial aggregate production quotas for the following controlled substances, expressed in grams of anhydrous acid or base, be established as follows:

Basic classEstablished initial 2003 quotas
Schedule I:
2,5-Dimethoxyamphetamine9,501,000
2,5-Dimethoxy-4-ethylamphetamine (DOET)2
3-Methylfentanyl4
3-Methylthiofentanyl2
3,4-Methylenedioxyamphetamine (MDA)15
3,4-Methylenedioxy-N-ethylamphetamine (MDEA)10
3,4-Methylenedioxymethamphetamine (MDMA)19
3,4,5-Trimethoxyamphetamine2
4-Bromo-2,5-Dimethoxyamphetamine (DOB)2
4-Bromo-2,5-Dimethoxyphenethylamine (2-CB)2
4-Methoxyamphetamine7
4-Methylaminorex2
4-Methyl-2,5-Dimethoxyamphetamine (DOM)2
5-Methoxy-3,4-Methylenedioxyamphetamine2
Acetyl-alpha-methylfentanyl2
Acetyldihydrocodeine2
Acetylmethadol2
Allylprodine2
Alphacetylmethadol7
Alpha-ethyltryptamine2
Alphameprodine2
Alphamethadol2
Alpha-methylfentanyl2
Alpha-methylthiofentanyl2
Aminorex17
Benzylmorphine2
Betacetylmethadol2
Beta-hydroxy-3-methylfentanyl2
Beta-hydroxyfentanyl2
Betameprodine2
Betamethadol2
Betaprodine2
Bufotenine2
Cathinone12
Codeine-N-oxide202
Diethyltryptamine2
Difenoxin9,000
Dihydromorphine1,101,000
Dimethyltryptamine3
Gamma-hydroxybutyric acid45,566,000
Heroin5
Hydromorphinol2
Hydroxypethidine2
Lysergic acid diethylamide (LSD)61
Marihuana840,000
Mescaline7
Methaqualone9
Methcathinone9
Methyldihydromorphine2
Morphine-N-oxide202
N,N-Dimethylamphetamine7
N-Ethyl-1-Phenylcyclohexylamine (PCE)5
Start Printed Page 77811
N-Ethylamphetamine7
N-Hydroxy-3,4-Methylenedioxyamphetamine2
Noracymethadol2
Norlevorphanol52
Normethadone7
Normorphine57
Para-fluorofentanyl2
Phenomorphan2
Pholcodine2
Propiram415,000
Psilocybin2
Psilocyn2
Tetrahydrocannabinols131,000
Thiofentanyl2
Trimeperidine2
Schedule II:
1-Phenylcyclohexylamine12
1-Piperidinocyclohexanecarbonitrile (PCC)10
Alfentanil700
Alphaprodine2
Amobarbital451,000
Amphetamine10,987,000
Cocaine171,000
Codeine (for sale)43,494,000
Codeine (for conversion)43,559,000
Dextropropoxyphene167,365,000
Dihydrocodeine741,000
Diphenoxylate501,000
Ecgonine31,000
Ethylmorphine12
Fentanyl733,000
Glutethimide1,002
Hydrocodone (for sale)29,243,000
Hydrocodone (for conversion)3,800,000
Hydromorphone1,409,000
Isomethadone12
Levo-alphacetylmethadol (LAAM)12
Levomethorphan2
Levorphanol8,600
Meperidine9,649,000
Metazocine1
Methadone (for sale)14,057,000
Methadone Intermediate17,393,000
Methamphetamine2,325,000
804,000 grams of levo-desoxyephedrine for use in a non-controlled, non-prescription product; 1,520,000 grams for methamphetamine for conversion to a Schedule III product; and 1,000 grams for methamphetamine (for sale)
Methylphenidate20,967,000
Morphine (for sale)18,218,000
Morphine (for conversion)110,774,000
Nabilone2
Noroxymorphone (for sale)40,000
Noroxymorphone (for conversion)4,400,000
Opium1,000,000
Oxycodone (for sale)34,482,000
Oxycodone (for conversion)700,000
Oxymorphone454,000
Pentobarbital27,728,000
Phencyclidine16
Phenmetrazine2
Phenylacetone21,975,000
Secobarbital1,100
Sufentanil3,000
Thebaine43,292,000

The Deputy Administrator further orders that aggregate production quotas for all other Schedules I and II controlled substances included in Sections 1308.11 and 1308.12 of Title 21 of the Code of Federal Regulations be established at zero.

The Office of Management and Budget has determined that notices of aggregate production quotas are not subject to centralized review under Executive Order 12866.

This action does not preempt or modify any provision of state law; nor does it impose enforcement responsibilities on any state; nor does it Start Printed Page 77812diminish the power of any state to enforce its own laws. Accordingly, this action does not have federalism implications warranting the application of Executive Order 13132.

The Deputy Administrator hereby certifies that this action will have no significant impact upon small entities whose interests must be considered under the Regulatory Flexibility Act, 5 U.S.C. 601 et seq. The establishment of aggregate production quotas for Schedules I and II controlled substances is mandated by law and by international treaty obligations. The quotas are necessary to provide for the estimated medical, scientific, research and industrial needs of the United States, for export requirements and the establishment and maintenance of reserve stocks. While aggregate production quotas are of primary importance to large manufacturers, their impact upon small entities is neither negative nor beneficial. Accordingly, the Deputy Administrator has determined that this action does not require a regulatory flexibility analysis.

This action meets the applicable standards set forth in Sections 3(a) and 3(b)(2) of Executive Order 12988 Civil Justice Reform.

This action will not result in the expenditure by State, local, and tribal governments, in the aggregate, or by the private sector, of $100,000,000 or more 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.

This action is not a major rule as defined by Section 804 of the Small Business Regulatory Enforcement Fairness Act of 1996. This action 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.

The Drug Enforcement Administration makes every effort to write clearly. If you have suggestions as to how to improve the clarity of this regulation, call or write Frank L. Sapienza, Chief, Drug & Chemical Evaluation Section, Office of Diversion Control, Drug Enforcement Administration, Washington, DC 20537, Telephone: (202) 307-7183.

Start Signature

Dated: December 13, 2002.

John B. Brown, III,

Deputy Administrator.

End Signature End Supplemental Information

[FR Doc. 02-31898 Filed 12-18-02; 8:45 am]

BILLING CODE 4410-09-P