[Federal Register Volume 69, Number 32 (Wednesday, February 18, 2004)]
[Notices]
[Pages 7657-7658]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 04-3477]


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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 October 20, 2003, Siegfried 
(USA), Inc., Industrial Park Road, Pennsville, New Jersey 08070, made 
application by renewal and on January 21, 2004, by letter to the Drug 
Enforcement Administration (DEA) for registration as a bulk 
manufacturer of the basic classes of controlled substances listed 
below:

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                    Drug                               Schedule
------------------------------------------------------------------------
Oxycodone (9143)...........................  II
Morphine (9300)............................  II
------------------------------------------------------------------------

    The firm plans to manufacture the listed controlled substances for 
distribution as bulk products to its customers.
    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 April 19, 
2004.


[[Page 7658]]


    Dated: February 4, 2004.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 04-3477 Filed 2-17-04; 8:45 am]
BILLING CODE 4410-09-M