[Federal Register Volume 67, Number 172 (Thursday, September 5, 2002)]
[Notices]
[Page 56857]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 02-22556]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

    Pursuant to section 1302.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on May 2, 2002, ISP Freetown 
Fine Chemicals, Inc., 238 South Main Street, Freetown, Massachusetts 
02702, made application by letter to the Drug Enforcement 
Administration (DEA) for registration as a bulk manufacturer of the 
basic classes of controlled substances listed below:

------------------------------------------------------------------------
                   Drug                               Schedule
------------------------------------------------------------------------
Methylphenidate (1724)....................  II
Dextropropoxyphene, bulk (non-dosage        II
 forms) (9273).
------------------------------------------------------------------------

    The firm plans to bulk manufacture the methylphenidate to produce a 
commercial product and manufacture the dextropropoxyphene to supply the 
generic market.
    Any other such applicant and any person who is presently registered 
with DEA to manufacture such substance 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 fled no later than November 4, 2002.

    Dated: August 23, 2002.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 02-22556 Filed 9-4-02; 8:45 am]
BILLING CODE 4410-09-M