[Federal Register Volume 70, Number 42 (Friday, March 4, 2005)]
[Notices]
[Page 10682]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 05-4206]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

    Pursuant to 21 CFR 1301.33(a), Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on January 5, 2005, Novus Fine 
Chemicals LLC, 611 Broad Street, Carlstadt, New Jersey 07072-1417, made 
application by renewal 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.
    The company plans to manufacture the listed controlled substance in 
bulk for distribution to its customers.
    Any other such applicant and any person who is presently registered 
with DEA to manufacture such a substance may file comments or 
objections to the issuance of the proposed registration pursuant to 21 
CFR 1301.33(a).
    Any such written comments or objections being sent via regular mail 
may be addressed, in quintuplicate, to the Deputy Assistant 
Administrator, Office of Diversion Control, Drug Enforcement 
Administration, Washington, DC 20537, Attention: DEA Federal Register 
Representative, Liaison and Policy Section (ODL); or any being sent via 
express mail should be sent to DEA Headquarters, Attention: DEA Federal 
Register Representative/ODL, 2401 Jefferson-Davis Highway, Alexandria, 
Virginia 22301; and must be filed no later than May 3, 2005.

    Dated: February 23, 2005.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 05-4206 Filed 3-3-05; 8:45 am]
BILLING CODE 4410-09-P