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Cody Laboratories, Inc.
FR Doc E6-6115 [Federal Register: April 25, 2006 (Volume 71, Number 79)]
[Notices] [Page 23948] From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr25ap06-115]
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 July 20, 2005, August 4, 2005 and September 2,
2005, Cody Laboratories, Inc., 601 Yellowstone Avenue, Cody, Wyoming 82414, made
application by letters to the Drug Enforcement Administration (DEA) for
registration as a bulk manufacturer of the basic classes of controlled
substances listed in Schedule II:
Drug
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Schedule
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Codeine (9050)
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II
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Dihydrocodeine (9120)
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II
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Methadone (9250)
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II
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Alfentanil (9737)
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II
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The company plans to manufacture 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 June 26,
2006.
Dated: April 18, 2006.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion
Control, Drug Enforcement Administration.
[FR Doc. E6-6115 Filed 4-24-06; 8:45 am]
BILLING CODE 4410-09-P
NOTICE: This is an
unofficial version. An official version of these publications may be obtained
directly from the Government Printing Office (GPO).
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