Notice of Registration - 2012
[Federal Register Volume 77, Number 63 (Monday, April 2, 2012)]
[Notices]
[Page 19718]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-7750]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration,
Norac Inc.
By Notice dated December 20, 2011, and published in the Federal
Register on December 29, 2011, 76 FR 81979, Norac Inc., 405 S. Motor
Avenue, Azusa, California 91702-3232, made application by renewal to
the Drug Enforcement Administration (DEA) to be registered as a bulk
manufacturer of the following basic classes of controlled substances:
| Drug |
Schedule |
| Gamma Hydroxybutyric Acid (2010) |
I |
| Tetrahydrocannabinols (7370) |
I |
| Methamphetamine (1105) |
II |
| Pentobarbital (2270) |
II |
| Nabilone (7379) |
II |
With regard to Gamma Hydroxybutyric Acid (2010),
Tetrahydrocannabinols (7370), and Methamphetamine (1105) only, the
company manufactures these controlled substances in bulk solely for
domestic distribution within the United States to customers engaged in
dosage-form manufacturing.
With regard to Nabilone (7379) only, the company presently
manufactures a small amount of this controlled substance in bulk solely
to conduct manufacturing internal process development. It is the
company's intention once the manufacturing process is refined to the
point that its Nabilone bulk product is available for commercial use,
the company will export the controlled substance in bulk solely to
customers engaged in dosage-form manufacturing outside the United
States. The company is aware of the requirement to obtain a DEA
registration as an exporter to conduct this activity.
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
Norac, Inc. to manufacture the listed basic classes of controlled
substances is consistent with the public interest at this time. DEA has
investigated Norac, 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 USC Sec. 823(a), 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 23, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2012-7750 Filed 3-30-12; 8:45 am]
BILLING CODE 4410-09-P
NOTICE: This is an unofficial version. An official version of this publication may be obtained
directly from the Government Printing Office (GPO). |