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60.fr.8251
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<ARTICLE>
Date="02/13/95"
Citation="60 FR 8251"
Group="legal"
Type="NOTICE"
Department="DEPARTMENT OF JUSTICE"
Agency="DRUG ENFORCEMENT ADMINISTRATION"
Subject="Proposed 1995 Aggregate Production Quota for a Schedule II Controlled Substance"
<HEADER>
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[DEA No. 129P]
Proposed 1995 Aggregate Production Quota for a Schedule II Controlled
Substance
AGENCY: Drug Enforcement Administration.
ACTION: Notice of a proposed 1995 aggregate production quota.
</HEADER>
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[DEA No. 129P]
Proposed 1995 Aggregate Production Quota for a Schedule II Controlled
Substance
AGENCY: Drug Enforcement Administration.
ACTION: Notice of a proposed 1995 aggregate production quota.
+
------------------------------------------------------------
SUMMARY: This notice proposes a 1995 aggregate production quota
for hydrocodone (for conversion), a controlled substance in
Schedule II of the Controlled Substances Act (CSA).
DATES: Comments or objections must be received on or before
March 15, 1995.
ADDRESSES: Send comments or objections to the Administrator,
Drug Enforcement Administration, Washington, DC 20537, Attn:
DEA Federal Register Representative/CCR.
FOR FURTHER INFORMATION CONTACT:
Howard McClain, Jr., Chief, Drug & Chemical Evaluation Section,
Drug Enforcement Administration, Washington, DC 20537, Telephone:
(202) 307-7183.
SUPPLEMENTARY INFORMATION: Section 306 of the Controlled Substances
Act (CSA) (21 U.S.C. 826) requires that the Attorney General
establish aggregate production quotas for controlled substances
in Schedules I and II each year. This responsibility has been
delegated to the Administrator of the DEA pursuant to 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 59 FR 23637 (May 6,
1994).
A company submitted an application for a manufacturing quota
for hydrocodone (for conversion) a Schedule II controlled substance.
Based on the review of this application and other information
available to the DEA, the Deputy Administrator of the DEA, under
the authority vested in the Attorney General by Section 306
of the Controlled Substances Act of 1970 (21 U.S.C. 826), delegated
to the Administrator by Section 0.100 of Title 28 of the Code
of Federal Regulations, and redelegated to the Deputy Administrator
pursuant to 59 FR 23637 (May 6, 1994), hereby proposes that
the 1995 aggregate production quota for the following controlled
substance, expressed in grams of anhydrous base, be established
as follows:
--------------------------------------------------------------+---------------
| Proposed
| 1995
Basic class | aggregate
| production
| quota
| (grams)
--------------------------------------------------------------+---------------
|
Hydrocodone (for conversion)................................. | 2,200,000
--------------------------------------------------------------+---------------
All interested persons are invited to submit comments or
objections, in writing, regarding this proposal. If a person
believes that one or more of these issues warrant a hearing,
the individual should so state and summarize the reasons for
this belief.
In the event that comments or objections to this proposal
raise one or more issues which the Administrator finds warrant
a hearing, the Administrator shall order a public hearing by
notice in the Federal Register, summarizing the issues to be
heard and setting the time for the hearing.
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 has been analyzed in accordance with the principles
and criteria contained in the Executive Order 12612 and it has
been determined that this matter does not have sufficient federalism
implications to warrant the preparation of a Federalism Assessment.
The Deputy Administrator hereby certifies that this action
will have no significant impact upon small entities within the
meaning of and intent of the Regulatory Flexibility Act, 5 U.S.C.,
601, et seq. The establishment of annual aggregate production
quotas for Schedules I and II controlled substances is mandated
by law and by international treaty obligations. 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.
Dated: February 6, 1995.
Stephen H. Green,
Deputy Administrator.
[FR Doc. 95-3456 Filed 2-10-95; 8:45 am]
BILLING CODE 4410-09-M
------------------------------------------------------
The Contents entry for this article reads as follows:
Schedules of controlled substances; production quotas:
Schedule II-
1995 proposed aggregate, 8251
</ARTICLE>
.