[Federal Register Volume 60, Number 139 (Thursday, July 20, 1995)]
[Notices]
[Page 37474]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-17889]



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DEPARTMENT OF JUSTICE
Drug Enforcement Administration


Manufacturer of Controlled Substances; Registration

    By Notice dated May 18, 1995, and published in the Federal Register 
on May 25, 1995, (60 FR 27790), Roche Diagnostic Systems, Inc., 1080 
U.S. Highway 202, Somerville, 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 (9250)..........................................           II 
Morphine (9300)...........................................           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, Sec. 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 14, 1995.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 95-17889 Filed 7-19-95; 8:45 am]
BILLING CODE 4410-09-M