[Federal Register Volume 70, Number 2 (Tuesday, January 4, 2005)]
[Notices]
[Page 390]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 05-76]



[[Page 390]]

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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 September 22, 2004 and 
October 29, 2004, Cedarburg Pharmaceuticals, Inc., 870 Badger Circle, 
Grafton, Wisconsin 53024, made application by letter to the Drug 
Enforcement Administration (DEA) to be registered as a bulk 
manufacturer of the basic classes of controlled substances listed in 
Schedule II.

------------------------------------------------------------------------
                    Drug                               Schedule
------------------------------------------------------------------------
Dihydrocodeine (9120)......................  II
Remifentanil (9739)........................  II
Sufentanil (9740)..........................  II
------------------------------------------------------------------------

    The company plans to manufacture the listed controlled substances 
in bulk 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: Federal Register Representative, 
Office of Liaison and Policy (ODLR) and must be filed no later than 
March 7, 2005.

    Dated: December 21, 2004.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 05-76 Filed 1-3-05; 8:45 am]
BILLING CODE 4410-09-P