[Federal Register Volume 70, Number 2 (Tuesday, January 4, 2005)]
[Notices]
[Page 393]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 05-69]


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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 November 16, 2004, Organichem 
Corporation, 33 Riverside Avenue, Rensselaer, New York 12144, made 
application by letter to the Drug Enforcement Administration (DEA) for 
registration as a bulk manufacturer of Hydrocodone (9193) and Fentanyl 
(9180), a basic class of controlled substances in Schedule II.
    The company plans to manufacture the listed controlled substances 
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 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: Federal Register Representative, 
Office of Liaison and Policy (ODLR) and must be filed no later than 
March 7, 2005.

    Dated: December 21, 2004.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 05-69 Filed 1-3-05; 8:45 am]
BILLING CODE 4410-09-P