98-3613. Manufacturer of Controlled Substances; Application

[Federal Register Volume 63, Number 29 (Thursday, February 12, 1998)]
[Notices]
[Page 7182]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 98-3613]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Application

    Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that by letter dated October 2, 1997, 
which was received for processing on October 26, 1997, Nycomed, Inc., 
33 Riverside Avenue, Rensselaer, New York 12144, made application to 
the Drug Enforcement Administration (DEA) for registration as a bulk 
manufacturer of methylphenidate (1724) a basic class of controlled 
substance listed in Schedule II.
    This bulk manufacture of methylphenidate is being conducted in 
conjunction and coordination with another bulk manufacturer.
    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: DEA Federal Register Representative 
(CCR), and must be filed no later than April 13, 1998.

    Dated: January 8, 1998.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 98-3613 Filed 2-11-98; 8:45 am]
BILLING CODE 4410-09-M