[Federal Register Volume 61, Number 105 (Thursday, May 30, 1996)]
[Notices]
[Page 27099]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-13561]



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DEPARTMENT OF JUSTICE

Manufacturer of Controlled Substances; Notice of Application

    Pursuant to Section 1301.43(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on April 14, 1996, Roche 
Diagnostic Systems, Inc., 1080 U.S. Highway 202, Somerville, New Jersey 
08876-3771, made application to the Drug Enforcement Administration 
(DEA) for registration as a bulk manufacturer of the basic classes of 
controlled substances listed below:

------------------------------------------------------------------------
                           Drug                               Schedule  
------------------------------------------------------------------------
Lysergic acid diethylamide (7315).........................            I 
Tetrahydrocannabinols (7370)..............................            I 
------------------------------------------------------------------------

    The firms plans to manufacture small quantities of the listed 
controlled substances for incorporation in drug of abuse detection 
kits.
    Any other such applicant and any person who is presently registered 
with DEA to manufacturer such substances may file comments or 
objections to the issuance of the above application.
    Any such comments or objections may be addressed, in quintuplicate, 
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 July 29, 1996.

    Dated: May 21, 1996.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 96-13561 Filed 5-29-96; 8:45 am]
BILLING CODE 4410-09-M