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Start Preamble
Pursuant to § 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on April 2, 2003, 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:
Start Printed Page 46227Drug 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 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 October 6, 2003.
Start SignatureDated: July 22, 2003.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.
[FR Doc. 03-19809 Filed 8-4-03; 8:45 am]
BILLING CODE 4410-09-M
Document Information
- Published:
- 08/05/2003
- Department:
- Drug Enforcement Administration
- Entry Type:
- Notice
- Document Number:
- 03-19809
- Pages:
- 46226-46227 (2 pages)
- PDF File:
- 03-19809.pdf