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Federal Register Notices > Notices of Application - 2003 > Cedarburg Pharmaceuticals, LLC

Notices of Application - 2003


FR Doc 03-3502
[Federal Register: February 12, 2003 (Volume 68, Number 29)]
[Notices]
[Page 7147]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr12fe03-59]


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 July 2, 2002, Cedarburg Pharmaceuticals, LLC, 870 Badger Circle, Grafton, Wisconsin 53024, 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
Tetrahydrocannabinols (7370) I
Oxycodone (9143) II
Hydromorphone (9150) II
Hydrocodone (9193) II

The firm will manufacturer these controlled substances for distribution to its customers.

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.

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 April 14, 2003.

Dated: February 5, 2003.

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

[FR Doc. 03-3502 Filed 2-11-03; 8:45 am]
BILLING CODE 4410-09-M

NOTICE: This is an unofficial version. An official version of these publications may be obtained directly from the Government Printing Office (GPO).


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