[Federal Register Volume 59, Number 95 (Wednesday, May 18, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-11998]


[[Page Unknown]]

[Federal Register: May 18, 1994]


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DEPARTMENT OF JUSTICE
 

Manufacturer of Controlled Substances; Registration

    By Notice dated March 21, 1994, and published in the Federal 
Register on April 1, 1994, (59 FR 15459), MD Pharmaceutical, Inc. 3501 
West Garry Avenue, Santa Ana, California 92704, made application to the 
Drug Enforcement Administration (DEA) to be registered as a bulk 
manufacturer of the basic classes of controlled substances listed 
below:

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

    No comments or objections have been received. Therefore, pursuant 
to Section 303 of the Comprehensive Drug Abuse Prevention and Control 
Act of 1970 and Title 21, Code of Federal Regulations, Section 
1301.54(e), the Deputy Assistant Administrator, Office of Diversion 
Control, hereby orders that the application submitted by the above firm 
for registration as a bulk manufacturer of the basic classes of 
controlled substances listed above is granted.

    Dated: May 11, 1994.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 94-11998 Filed 5-17-94; 8:45 am]
BILLING CODE 4410-09-M