[Federal Register: April 27, 1999 (Volume 64, Number 80)]
[Notices]               
[Page 22645-22646]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr27ap99-82]

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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

 
Manufacturer of Controlled Substances Notice of Application

    Pursuant to Section 1301.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on January 25, 1999, Stepan 
Company, Natural Products Department, 100 W. Hunter Avenue, Maywood, 
New Jersey 07607, made application by renewal 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
------------------------------------------------------------------------

    The firm plans to manufacture bulk controlled substances 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 proposed registration.
    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, DC 20537, Attention: DEA Federal Register Representative 
(CCR), and must be filed no later than (60 days from publication).


[[Page 22646]]


    Dated: April 12, 1999.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 99-10512 Filed 4-20-99; 8:45 am]
BILLING CODE 4410-09-M