Notice of Registration - 2012
[Federal Register Volume 77, Number 161 (Monday, August 20, 2012)]
[Notices]
[Page 50163]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-20369]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances, Notice of Registration,
Cody Laboratories, Inc.
By Notice dated March 8, 2012, and published in the Federal
Register on March 20, 2012, 77 FR 16263, Cody Laboratories, Inc., 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 following basic classes of controlled substances:
Drug |
Schedule |
4-Anilino-N-phenethyl-4-piperidine (8333) |
II |
Thebaine (9333) |
II |
The company plans on manufacturing the listed controlled substances
as bulk intermediates for distribution 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, Inc. to manufacture the
listed basic classes of controlled substances is consistent with the
public interest at this time. DEA has investigated Cody Laboratories,
Inc. 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: August 7, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2012-20369 Filed 8-17-12; 8:45 am]
BILLING CODE 4410-09-P
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