[Federal Register Volume 60, Number 16 (Wednesday, January 25, 1995)]
[Notices]
[Page 4926]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-1773]



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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 December 20, 1994, MD 
Pharmaceutical, Inc., 3501 West Garry Avenue, Santa Ana, California 
92704, made application to the Drug Enforcement Administration (DEA) 
for registration as a bulk manufacturer of the basic classes of 
controlled substances listed below:

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                             Drug                               Schedule
------------------------------------------------------------------------
Methylphenidate (1724).......................................         II
Diphenoxylate (9170).........................................         II
------------------------------------------------------------------------

    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, D.C. 20537, Attention: DEA Federal Register 
Representative (CCR), and must be filed no later than February 24, 
1995.

    Dated: January 17, 1995.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 95-1773 Filed 1-24-95; 8:45 am]
BILLING CODE 4410-09-M