[Federal Register Volume 60, Number 40 (Wednesday, March 1, 1995)]
[Notices]
[Pages 11115-11116]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-4934]



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DEPARTMENT OF JUSTICE

Manufacturer of Controlled Substances; Application

    Pursuant to Sec. 1301.43(a) of title 21 of the Code of Federal 
Regulations (CFR), this is notice that on January 24, 1995, Organix 
Inc., 65 Cummings Park, Woburn, Massachusetts 01801, made application 
to the Drug Enforcement [[Page 11116]] Administration (DEA) for 
registration as a bulk manufacturer of the basic classes of controlled 
substances listed below:

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                           Drug                               Schedule  
------------------------------------------------------------------------
Tetrahydrocannabinols (7370)..............................  I           
Morphine (9300)...........................................  II          
------------------------------------------------------------------------

    The firm plans to manufacture Tetrahydrocannabinols and a 
derivative of Morphine for use in diagnostic kits.
    Any other such applicant and any person who is presently registered 
with DEA to manufacture such substances may file comments or objections 
to the issuance of the above application and may also file a written 
request for a hearing thereon in accordance with 21 CFR 1301.54 and in 
the form prescribed by 21 CFR 1316.47.
    Any such comments, objections, or requests for a hearing may be 
addressed to the Deputy Assistant Administrator, Office of Diversion 
Control, Drug Enforcement Administration, United States Department of 
Justice, Washington, DC 20537, Attention: DEA Federal Register 
Representative (CCR), and must be filed no later than March 31, 1995.

    Dated: February 17, 1995.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 95-4934 Filed 2-28-95; 8:45 am]
BILLING CODE 4410-09-M