[Federal Register Volume 60, Number 206 (Wednesday, October 25, 1995)]
[Notices]
[Page 54708]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-26448]



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DEPARTMENT OF JUSTICE

Manufacturer of Controller 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 September 20, 1995, Nycomed 
Inc., 33 Riverside Avenue, Rensselaer, New York 12144, made a written 
request to the Drug Enforcement Administration (DEA) for registration 
as a bulk manufacturer of the Schedule II controlled substance 
Meperidine (9230).
    The firm plans to manufacture bulk product 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 on 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, D.C. 
20537, Attention: DEA Federal Register Representative (CCR), and must 
be filed no later than December 26, 1995.

    Dated: October 19, 1995.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 95-26448 Filed 10-24-95; 8:45 am]
BILLING CODE 4410-09-M