[Federal Register Volume 66, Number 245 (Thursday, December 20, 2001)]
[Notices]
[Page 65744]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 01-31279]


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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 September 4, 2001, 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..................................  II
Hydromorphone (9150).......................  II
Hydrocodone (9193).........................  II
------------------------------------------------------------------------

    The firm will manufacture these controlled substances for another 
firm.
    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 February 19, 2002.

    Dated: November 26, 2001.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control Drug 
Enforcement Administration.
[FR Doc. 01-31279 Filed 12-19-01; 8:45 am]
BILLING CODE 4410-09-M