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

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Manufacturers Notice of Application - 2004

FR Doc 04-12461 [Federal Register: June 3, 2004 (Volume 69, Number 107)] [Notices] [Page 31411] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr03jn04-86]


DEPARTMENT OF JUSTICE

Drug Enforcement Administration

Manufacturer of Controlled Substances; Notice of Application

Pursuant to section 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on March 17, 2004, Boehringer Ingelheim Chemicals Inc., 2820 N. Normandy Drive, 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.

DrugĀ  Schedule
Amphetamine (1100) II
Methylphenidate (1724) II
Methadone (9250) II
Methadone Intermediate (9254) II
Dextropropoxyphene, bulk (non-dosage forms)(9273) II
Levo-alphacetylmethadol (9648) II
Fentanyl (9801) II

The firm plans to 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: Federal Register Representative, Office of Chief Counsel (CCD) and must be filed no later than August 2, 2004.

Dated: May 5, 2004.

William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.

[FR Doc. 04-12461 Filed 6-2-04; 8:45 am]

BILLING CODE 4410-09-M

 

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