[Federal Register Volume 60, Number 76 (Thursday, April 20, 1995)]
[Notices]
[Pages 19779-19780]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-9715]



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DEPARTMENT OF JUSTICE
Drug Enforcement Administration


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 February 23, 1995, Stepan 
Company, Natural Products Department, 100 W. Hunter Avenue, Maywood, 
New Jersey 07607, made application to the Drug Enforcement 
Administration (DEA) for registration as a bulk manufacturer of the 
basic classes of controlled substances listed below:

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                             Drug                               Schedule
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Cocaine (9041)................................................  II      
Benzoylecgonine (9180)........................................  II      
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    The firms plans to manufacture bulk Cocaine for distribution to its 
customers.
    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, D.C. 20537, Attention: DEA Federal Register 
Representative (CCR), and must be filed no later than May 22, 1995.

    [[Page 19780]] Dated: April 7, 1995.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 95-9715 Filed 4-19-95; 8:45 am]
BILLING CODE 4410-09-M