[Federal Register Volume 66, Number 7 (Wednesday, January 10, 2001)]
[Notices]
[Page 2004]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 01-750]



[[Page 2004]]

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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 October 26, 2000, Medeva 
Pharmaceuticals CA, Inc., 3501 West Garry Avenue, Santa Ana, California 
92704, made application by renewal to the Drug Enforcement 
Administration (DEA) to be registered as a bulk manufacturer of 
methylphenidate (1724), a basic class of controlled substance listed in 
Schedule II.
    The firm plans to manufacture methyphenidate to make finished 
dosage forms 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: 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. 01-750 Filed 1-9-01; 8:45 am]
BILLING CODE 4410-09-M