Diversion Control Division, US Department of Justice, Drug Enforcement Administration

Manufacturers Notice of Registration - 2009

FR Doc E9-25885[Federal Register: October 28, 2009 (Volume 74, Number 207)] [Notices] [Page 55589-55590] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr28oc09-117]


DEPARTMENT OF JUSTICE

Drug Enforcement Administration

Manufacturer of Controlled Substances; Notice of Registration

By Notice dated February 5, 2009 and published in the Federal Register on February 11, 2009, (74 FR 6921), Siegfried (USA), Inc., 33 Industrial Park Road, Pennsville, New Jersey 08070, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled substances listed in schedules I and II:

Drug Schedule
Dihydromorphine (9145)  I
Amphetamine (1100)  II
Methylphenidate (1724)  II
Amobarbital (2125)  II
Pentobarbital (2270)  II
Secobarbital (2315)  II
Glutethimide (2550)  II
Codeine (9050)  II
Oxycodone (9143)  II
Hydromorphone (9150)  II
Hydrocodone (9193)  II
Methadone (9250)  II
Methadone intermediate (9254)  II
Dextropropoxyphene, bulk (non-dosage forms) (9273)  II
Morphine (9300)  II
Oripavine (9330)  II
Oxymorphone (9652)  II

The company plans to manufacture the listed controlled substances in bulk 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 Siegfried (USA), Inc. to manufacture the listed basic classes of controlled substances is consistent with the public interest at this time. DEA has investigated Siegfried (USA), 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.

[[Page 55590]]

Dated: October 16, 2009.

Joseph T. Rannazzisi, 
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.

[FR Doc. E9-25885 Filed 10-27-09; 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 Publishing Office (GPO).

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