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Federal Register Notices > Notices of Registration - 2006  > Cambrex North Brunswick, Inc.

Notice of Registration - 2006 


FR Doc E6-21878 [Federal Register: December 22, 2006 (Volume 71, Number 246)] [Notices] [Page 77063-77064] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr22de06-104]


DEPARTMENT OF JUSTICE

Drug Enforcement Administration

Manufacturer of Controlled Substances; Notice of Registration

By Notice dated August 15, 2006, and published in the Federal Register on August 22, 2006, (71 FR 48945-48946), Cambrex North Brunswick, Inc., Technology Centre of New Jersey, 661 Highway One, North Brunswick, New Jersey 08902, 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 schedule I and II:

Drug  Schedule
N-Ethylamphetamine (1475)  I
Tetrahydrocannabinols (7370)  I
2,5-Dimethoxyamphetamine (7396)  I
3,4-Methylenedioxyamphetamine (7400)  I
4-Methoxyamphetamine (7411)  I
Amphetamine (1100)  II
Methamphetamine (1105)  II
Methylphenidate (1724)  II
Pentobarbital (2270)  II
Phenylacetone (8501)  II
Hydromorphone (9150)  II
Hydrocodone (9193)  II
Methadone (9250)  II
Methadone Intermediate (9254)  II
Morphine (9300)  II
Sufentanil (9740)  II
Fentanyl (9801)  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 Cambrex North Brunswick, Inc. to manufacture the listed basic classes of controlled substances is consistent with the public interest at this time. DEA has investigated Cambrex North Brunswick, 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

[[Page 77064]]

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: December 14, 2006.

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

[FR Doc. E6-21878 Filed 12-21-06; 8:45 am]

BILLING CODE 4410-09-P

NOTICE: This is an unofficial version. An official version of these publications may be obtained directly from the Government Printing Office (GPO).

 


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