Manufacturer of Controlled Substances; Notice of Registration

Download PDF
Federal RegisterJun 3, 2004
69 Fed. Reg. 31411 (Jun. 3, 2004)

By Notice dated February 4, 2004, and published in the Federal Register on February 18, 2004, (69 FR 7655), Cambrex Charles City, Inc., 1205 11th Street, Charles City, Iowa 50619, made application by renewal to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of the basic classes of controlled substances listed below:

Drug Schedule
Amphetamaine (1100) II
Methylphenidate (1724) II
Dextropropoxyphene (9273) II

The firm plans to manufacture bulk controlled substances for distribution to its customers.

No comments or objections have been received. DEA has considered the factors in Title 21, United States Code, section 823(a) and determined that the registration of Cambrex Charles City, Inc. to manufacture the listed controlled substances is consistent with the public interest at this time. DEA has investigated Cambrex Charles City, Inc. to ensure that the company's registration is consistent with the public interest. This 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 28 CFR 0.100 and 0.104, the Deputy Assistant Administrator, Office of Diversion Control, hereby orders that the application submitted by the above firm for registration as a bulk manufacturer of the basis classes of controlled substances listed as granted.

Dated: May 21, 2004.

William J. Walker,

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

[FR Doc. 04-12456 Filed 6-2-04; 8:45 am]

BILLING CODE 4410-09-M