[Federal Register Volume 63, Number 196 (Friday, October 9, 1998)]
[Notices]
[Page 54492]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 98-27106]


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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 July 28, 1998, Nycomed, Inc., 
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:

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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 perform a chemical isolation 
process on methylphenidate which has been manufactured by another bulk 
manufacturer of methylphenidate.
    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, D.C. 20537, Attention: DEA Federal Register Representative 
(CCR), and must be filed no later than December 8, 1998.

    Dated: October 1, 1998.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 98-27106 Filed 10-8-98; 8:45 am]
BILLING CODE 4410-09-M