[Federal Register Volume 65, Number 55 (Tuesday, March 21, 2000)]
[Notices]
[Page 15178]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 00-6984]


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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 December 27, 1999, Organichem 
Corporation, 33 Riverside Avenue, Renssalaer, 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:

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                    Drug                               Schedule
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Methylphenidate (1724).....................  II
Meperidine (9230)..........................  II
------------------------------------------------------------------------

    The firm plans to manufacture meperidine as bulk product for 
distribution to its customers and to manufacture methylphenidate for 
distribution to a customer.
    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, D.C. 20537, Attention: DEA Federal Register Representative 
(CCR), and must be filed no later than May 22, 2000.

    March 13, 2000.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 00-6984 Filed 3-20-00; 8:45 am]
BILLING CODE 4410-09-M