Manufacturer of Controlled Substances; Registrations

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Federal Register: March 5, 2010 (Volume 75, Number 43)

Notices

Page 10313-10314

From the Federal Register Online via GPO Access [wais.access.gpo.gov]

DOCID:fr05mr10-120

DEPARTMENT OF JUSTICE

Drug Enforcement Administration

Manufacturer of Controlled Substances; Notice of Registration

By Notice dated October 16, 2009, and published in the Federal

Register on October 28, 2009, (74 FR 55586), Lonza Riverside, 900 River

Road, Conshohocken, Pennsylvania 19428, 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

Gamma hydroxybutyric acid (2010)........... I

Amphetamine (1100)......................... II

Methylphenidate (1724)..................... II

The company plans to manufacture bulk products for finished dosage units and 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

Lonza Riverside to manufacture the listed basic classes of controlled substances is consistent with the public interest at this time. DEA has investigated Lonza Riverside to ensure

Page 10314

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: February 26, 2010.

Joseph T. Rannazzisi,

Deputy Assistant Administrator, Office of Diversion Control, Drug

Enforcement Administration.

FR Doc. 2010-4728 Filed 3-4-10; 8:45 am

BILLING CODE 4410-09-P

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