[Federal Register Volume 74, Number 122 (Friday, June 26, 2009)]
[Notices]
[Page 30621]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: E9-15235]


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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 March 19, 2009, Wildlife 
Laboratories Inc., 1401 Duff Drive, Suite 400, Fort Collins, Colorado 
80524, made application 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 will 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 a substance, 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 25, 2009.

    Dated: June 22, 2009.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. E9-15235 Filed 6-25-09; 8:45 am]
BILLING CODE 4410-09-P