[Federal Register Volume 68, Number 150 (Tuesday, August 5, 2003)]
[Notices]
[Page 46227]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 03-19810]


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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 May 23, 2003, Wildlife 
Laboratories, Inc., 1401 Duff Drive, Suite 600, Fort Collins, Colorado 
80524, made application by renewal to the Drug Enforcement 
Administration (DEA) for registration as a bulk manufacturer of 
Carfentanil (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 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 Assistance Administrator, Office of Diversion Control, 
Drug Enforcement Administration, United States Department of Justice, 
Washington, DC 20537, Attention: Federal Register Representative, 
Office of Chief Counsel (CCD) and must be filed no later than October 
6, 2003.

    Dated: July 22, 2003.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 03-19810 Filed 8-4-03; 8:45 am]
BILLING CODE 4410-09-M