[Federal Register: March 19, 2008 (Volume 73, Number 54)]
[Notices]
[Page 14842-14843]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr19mr08-95]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated November 6, 2007 and published in the Federal
Register on November 16, 2007 (72 FR 64677-64678), Cody Laboratories,
601 Yellowstone Avenue, Cody, Wyoming 82414, made application by letter
to the Drug Enforcement Administration (DEA) to be registered as a bulk
manufacturer of the basic classes of controlled substances listed in
schedule II:
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Drug Schedule
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Codeine (9050)............................. II
[[Page 14843]]
Ecgonine (9180)............................ II
Hydrocodone (9193)......................... II
Morphine (9300)............................ II
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The company plans on manufacturing the listed controlled substances
in bulk for sale to its customers.
No comments or objections have been received. DEA has considered
the factors in 21 U.S.C. 823(a) and determined that the registration of
Cody Laboratories to manufacture the listed basic classes of controlled
substances is consistent with the public interest at this time. DEA has
investigated Cody Laboratories to ensure that the company's
registration is consistent with the public interest. The investigation
has included inspection and testing of the company's physical security
systems, verification of the company's compliance with State and local
laws, and a review of the company's background and history. Therefore,
pursuant to 21 U.S.C. 823, and in accordance with 21 CFR 1301.33, the
above named company is granted registration as a bulk manufacturer of
the basic classes of controlled substances listed.
Dated: March 10, 2008.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E8-5506 Filed 3-18-08; 8:45 am]
BILLING CODE 4410-09-P