[Federal Register Volume 77, Number 219 (Tuesday, November 13, 2012)]
[Notices]
[Pages 67676-67677]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2012-27568]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration; 
Wildlife Laboratories, Inc.

    By Notice dated April 17, 2012, and published in the Federal 
Register on July 31, 2012, 77 FR 45378, Wildlife Laboratories, Inc., 
1230 W. Ash Street, Suite D, Windsor, Colorado 80550, 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.
    No comments or objections have been received. DEA has considered 
the factors in 21 U.S.C. 823(a), and determined that the registration 
of Wildlife Laboratories, Inc., to manufacture the listed basic class 
of controlled substance is consistent with the public interest at this 
time. DEA has investigated Wildlife Laboratories, Inc., to ensure that 
the company's registration is consistent with the public interest. The 
investigation has included inspection and testing of the company's 
physical security systems, verification of the company's compliance 
with state and local laws, and a review of the company's background and 
history.
    Therefore, pursuant to 21 U.S.C. 823(a), and in accordance with 21 
CFR

[[Page 67677]]

1301.33, the above named company is granted registration as a bulk 
manufacturer of the basic class of controlled substance listed.

    Dated: November 5, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 2012-27568 Filed 11-9-12; 8:45 am]
BILLING CODE 4410-09-P