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

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Manufacturers Notice of Application - 2003

FR Doc 03-8583 [Federal Register: April 9, 2003 (Volume 68, Number 68)] [Notices] [Page 17402-17403] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr09ap03-80]


DEPARTMENT OF JUSTICE

Drug Enforcement Administration

Manufacturer of Controlled Substances; Notice of Application

Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on February 14, 2003, Boehringer Ingelheim Chemicals, Inc., 2820 N. Normandy Drive, Petersburg, Virginia 23805, made application by renewal, and on November 27, 2002, made application by renewal, and on November 27, 2002, made application by letter to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of the basic classes of controlled substances listed below:

Drug Schedule
Amphetamine (1100) II
Methadone (9250) II
Methadone-intermediate (9254) II
Methylphenidate (1724) II
Levo-aphacetylmethadol (9648) II
Fentanyl (9801) II
Dextropropoxphene (9273) 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 substances may file comments or objections to the issuance of the proposed registration.

[[Page 17403]]

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: Drug Operations Section, Domestic Drug Unit (ODOD) and must be filed no later than June 9, 2003.

Dated: March 21, 2003.

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

[FR Doc. 03-8583 Filed 4-8-03; 8:45 am]

BILLING CODE 4410-09-M

 

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