[Federal Register: January 4, 2005 (Volume 70, Number 2)]
[Notices]
[Page 388-389]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr04ja05-71]
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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 October 28, 2004, Cambrex
Charles City, Inc., 1205 11th Street, Charles City, Iowa 50616, made
application by renewal and on October 13, 2004 by letter to the Drug
Enforcement Administration (DEA) for registration as a bulk
manufacturer of the basic classes of controlled substances listed:
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Drug Schedule
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Amphetamine (1100).......................... II
Methylphenidate (1724)...................... II
Dextropropoxyphene (9273)................... II
Fentanyl (9801)............................. II
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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.
[[Page 389]]
Dated: December 21, 2004.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 05-72 Filed 1-3-05; 8:45 am]
BILLING CODE 4410-09-P