Manufacturer of Controlled Substances; Notice of Application

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Federal RegisterApr 26, 2004
69 Fed. Reg. 22566 (Apr. 26, 2004)

Pursuant to § 1301.33(a) of title 21 of the code of Federal Regulations (CFR), this is notice that on February 18, 2004, Penick, Corporation, 158 Mount Olivet Avenue, Newark, New Jersey 07114, made application to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of the basic classes of controlled substances listed below:

Drug Schedule
Cocaine (9041) II
Codeine (9050) II
Dihydrocodeine (9120) II
Oxycodone (9143) II
Hydromorphone (9150) II
Diphenoxylate (9170) II
Ecgonine (9180) II
Hydrocodone (9193) II
Morphine (9300) II
Thebaine (9333) II
Oxymorphone (9652) II

The firm plans to manufacture bulk controlled substances and non-controlled substance flavor extracts.

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.

Any such comments or objections may be addressed, in quintuplicate, to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, United States Department of Justice, Washington, DC 20537, Attention: Federal Register Representative, Office of Chief Counsel (CCD), and must be filed no later than June 25, 2004.

Dated: April 9, 2004

William J. Walker,

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

[FR Doc. 04-9326 Filed 4-23-04; 8:45 am]

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