77 FR 228 pg. 70825 - Manufacturer of Controlled Substances;Notice of Application; Norac
Type: NOTICEVolume: 77Number: 228Page: 70825
FR document: [FR Doc. 2012-28662 Filed 11-26-12; 8:45 am]
Agency: Justice Department
Sub Agency: Drug Enforcement Administration
Official PDF Version: PDF Version
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances;Notice of Application; Norac
Pursuant to § 1301.33(a), Title 21 of the Code of Federal Regulations (CFR), this is notice that on October 31, 2012, Norac, DBA: Norac Pharma, 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), the company presently manufactures a small amount of this controlled substance in bulk solely to conduct manufacturing process development internally within the company. It is the company's intention that, when 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.
Any other such applicant, and any person who is presently registered with DEA to manufacture such substances, 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 should be addressed, in quintuplicate, to the Drug Enforcement Administration, Office of Diversion Control, Federal Register Representative (ODL), 8701 Morrissette Drive,Springfield, Virginia 22152; and must be filed no later than January 28, 2013.
Dated: November 19, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator,Office of Diversion Control,Drug Enforcement Administration.
[FR Doc. 2012-28662 Filed 11-26-12; 8:45 am]
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