[Federal Register Volume 75, Number 123 (Monday, June 28, 2010)]
[Notices]
[Page 36683]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2010-15527]



[[Page 36683]]

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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 March 11, 2010, Wildlife 
Laboratories Inc., 1401 Duff Drive, Suite 400, Fort Collins, Colorado 
80524, made application by renewal to the Drug Enforcement 
Administration (DEA) to be registered as a bulk manufacturer of 
Carfentanil (9743), a basic class of controlled substance listed in 
schedule II.
    The company plans to manufacture the above listed controlled 
substance for sale to veterinary pharmacies, zoos, and for other animal 
and wildlife applications.
    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 pursuant to 
21 CFR 1301.33(a).
    Any such comments or objections should be addressed, in 
quintuplicate, to the Drug Enforcement Administration, Office of 
Diversion Control, Federal Register Representative (ODL), 8701 
Morrissette Drive, Springfield, Virginia 22152; and must be filed no 
later than August 27, 2010.

    Dated: June 17, 2010.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 2010-15527 Filed 6-25-10; 8:45 am]
BILLING CODE 4410-09-P