[Federal Register Volume 66, Number 7 (Wednesday, January 10, 2001)]
[Notices]
[Page 2005]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 01-749]


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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 25, 2000, 
Organichem Corporation, 33 Riverside Avenue, Rensselaer, New York 
12144, 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
------------------------------------------------------------------------
Amphetamine (1100).........................  II
Methylphenidate (1724).....................  II
Pentobarbital (2270).......................  II
Meperidine (9230)..........................  II
------------------------------------------------------------------------

    The firm plans to manufacture bulk products for distribution to its 
customers.
    Any other such applicants 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 March 12, 2001.

    Dated: December 4, 2000.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 01-749 Filed 1-9-01; 8:45 am]
BILLING CODE 4410-09-M