[Federal Register Volume 69, Number 83 (Thursday, April 29, 2004)]
[Notices]
[Page 23538]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 04-9658]


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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 November 30, 2003, Lonza 
Riverside, 900 River Road, Conshohocken, Pennsylvania 19428, 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:

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                    Drug                               Schedule
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Gamma hydroxybutyric acid (2010)...........  I
Amphetamine (1100).........................  II
Methylphenidate (1724).....................  II
------------------------------------------------------------------------

    The firm plans to produce bulk products for finished dosage units 
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 Chief Counsel (CCD) and must be filed no later than June 28, 
2004.

    Dated: March 29, 2004.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 04-9658 Filed 4-28-04; 8:45 am]
BILLING CODE 4410-09-M