[Federal Register Volume 66, Number 201 (Wednesday, October 17, 2001)]
[Notices]
[Page 52782]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 01-26015]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

    Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on April 30, 2001, Wildlife 
Laboratories, Inc., 1401 Duff Drive, Suite 600, Ft. Collins, Colorado 
80524, made application by renewal to the Drug Enforcement 
Administration (DEA) for registration as a bulk manufacturer of 
carfentanial (9743), a basic class of controlled substance listed in 
Schedule II.
    The firm plans to manufacture the listed controlled substance for 
distribution to its customers.
    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 filed no later than December 17, 2001.

    Dated: October 5, 2001.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 01-26015 Filed 10-16-01; 8:45 am]
BILLING CODE 4410-09-M