[Federal Register Volume 59, Number 124 (Wednesday, June 29, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-15707]


[[Page Unknown]]

[Federal Register: June 29, 1994]


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DEPARTMENT OF JUSTICE
Drug Enforcement Administration

 

Manufacturer of Controlled Substances; Notice of Application

    Pursuant to Section 1301.43(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on June 1, 1994, Penick 
Corporation, 158 Mount Olivet Avenue, Newark, New Jersey 07114, made 
written request 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 issue 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 July 29, 1994.

    Dated: June 22, 1994.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 94-15707 Filed 6-28-94; 8:45 am]
BILLING CODE 4410-09-M