[Federal Register Volume 76, Number 105 (Wednesday, June 1, 2011)]
[Notices]
[Pages 31638-31639]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2011-13487]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

    Pursuant to Sec.  1301.33(a), Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on February 15, 2011, 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 substance, may file comments or 
objections to the issuance of the proposed registration pursuant to 21 
CFR 1301.33(a).

[[Page 31639]]

    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 1, 2011.

    Dated: May 25, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 2011-13487 Filed 5-31-11; 8:45 am]
BILLING CODE 4410-09-P