Diversion Control Division, US Department of Justice, Drug Enforcement Administration

Manufacturers Notice of Application - 2001

[Federal Register: October 17, 2001 (Volume 66, Number 201)] [Notices] [Page 52780-52781] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr17oc01-105] 


DEPARTMENT OF JUSTICE

Drug Enforcement Administration

Manufacturer of Controlled Substances; Notice of Application

Pursuant to § 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on April 23, 2001, B.I. Chemical Inc., 2820 N. Normandy Drive,

[[Page 52781]]

Petersburg, Virginia 23805, made application by renewal to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of the basic classes of controlled substances listed below:

Drug  Schedule
Methylphenidate (1724) II
Amphetamine (1100) II
Methadone (9250) II
Methadone-intermediate (9254) II
Levo-alphacetylmethadol (LAAM) (9648) II

The firm plans to bulk manufacture the listed controlled substances for formulation into finished pharmaceuticals.

Any other such applicant and any person who is presently registered with DEA to manufacture such substance may file comments or objections to the issuance of the proposed registration.

Any such comments or objections may be addressed, in quintuplicate, to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, United States Department of Justice, Washington, DC. 20537, Attention: DEA Federal Register Representative (CCR), and must be filed no later than December 17, 2001.

Dated: October 5, 2001.

Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.

[FR Doc. 01-26017 Filed 10-16-01; 8:45 am]

BILLING CODE 4410-09-M

 

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