[Federal Register Volume 60, Number 49 (Tuesday, March 14, 1995)]
[Notices]
[Page 13735]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-6220]



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DEPARTMENT OF JUSTICE

Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated January 17, 1995, and published in the Federal 
Register on January 25, 1995, (60 FR 4926), 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: March 8, 1995.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 95-6220 Filed 3-13-95; 8:45 am]
BILLING CODE 4410-09-M