[Federal Register Volume 59, Number 144 (Thursday, July 28, 1994)]
[Unknown Section]
[Page ]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-18343]


[Federal Register: July 28, 1994]


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DEPARTMENT OF JUSTICE

Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated May 3, 1994, and published in the Federal Register 
on May 10, 1994, (59 FR 24184), Roche Diagnostic Systems, Inc., 1080 
U.S. Highway 202, Branchburg, New Jersey 08876, 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  
------------------------------------------------------------------------
Lysergic acid diethylamide (7315)........................  I            
Tetrahydrocannabinols (7370).............................  I            
Phencyclidine (7471).....................................  II           
Methadone................................................  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: July 20, 1994.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 94-18343 Filed 7-27-94; 8:45 am]
BILLING CODE 4410-09-M