[Federal Register Volume 60, Number 162 (Tuesday, August 22, 1995)]
[Notices]
[Page 43613]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-20753]



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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


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 July 20, 1995, Ganes 
Chemicals, Inc., Industrial park Road, Pennsville, New Jersey 08070, 
made written request to the Drug Enforcement Administration (DEA) for 
registration as a bulk manufacturer of the Schedule II controlled 
substance Methylphenidate (1724).
    The firm plans to manufacture the Methylphenidate for distribution 
as a bulk product 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.
    Any such comments or objections 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 October 23, 1995.

    Dated: August 14, 1995.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 95-20753 Filed 8-21-95; 8:45 am]
BILLING CODE 4410-09-M