[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