94-17525. Manufacturer of Controlled Substances; Notice of Application
[Federal Register Volume 59, Number 137 (Tuesday, July 19, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-17525]
[[Page Unknown]]
[Federal Register: July 19, 1994]
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DEPARTMENT OF JUSTICE
Manufacturer of Controlled Substances; Notice of Application
Pursuant to Sec. 1301.43(a) of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on June 24, 1994, Abbott
Laboratories, 14th Street & Sheridan Road, Attn: Customer Service D-
345, North Chicago, Illinois 60064, made application to the Drug
Enforcement Administration (DEA) for registration as a bulk
manufacturer of the Schedule II controlled substance
Dextropropoxyphene, bulk (non-dosage forms) (9273).
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 above application and may also file a written
request for a hearing thereon in accordance with 21 CFR 1301.54 and in
the form prescribed by 21 CFR 1316.47.
Any such comments, objections or requests for a hearing may be
addressed to the Deputy Assistant Administrator, Office of Diversion
Control, Drug Enforcement Administration, United States Department of
Justice, Washington, DC 20537, Attention: DEA Federal Register
Representative (CCR), and must be filed no later than August 18, 1994.
Dated: July 11, 1994.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 94-17525 Filed 7-18-94; 8:45 am]
BILLING CODE 4410-09-M
Document Information
- Published:
- 07/19/1994
- Department:
- Justice Department
- Entry Type:
- Uncategorized Document
- Document Number:
- 94-17525
- Pages:
- 0-0 (1 pages)
- Docket Numbers:
- Federal Register: July 19, 1994