[Federal Register Volume 59, Number 156 (Monday, August 15, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-19818]


[[Page Unknown]]

[Federal Register: August 15, 1994]


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DEPARTMENT OF JUSTICE
Drug Enforcement Administration

 

Manufacturer of Controlled Substances; Application

    Pursuant to Sec. 1301.43(a) of title 21 of the Code of Federal 
Regulations (CFR), this is notice that on July 7, 1994, Ciba-Geigy 
Corporation, Pharmaceuticals Division Regulatory Compliance, 556 Morris 
Avenue, Summit, New Jersey 07901, made application to the Drug 
Enforcement Administration (DEA) for registration as a bulk 
manufacturer of the Schedule II controlled substance Methylphenidate 
(1724).
    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 September 14, 
1994.

    Dated: August 5, 1994.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 94-19818 Filed 8-12-94; 8:45 am]
BILLING CODE 4410-09-M