Justia Regulation Tracker

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[Federal Register: October 28, 2009 (Volume 74, Number 207)]
[Notices]               
[Page 55589]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr28oc09-116]                         

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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

 
Manufacturer of Controlled Substances Notice of Registration

    By Notice dated June 22, 2009, and published in the Federal 
Register on June 26, 2009, (74 FR 30621), 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.
    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(es) of 
controlled substance(s) 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, and in accordance with 
21 CFR 1301.33, the above named company is granted registration as a 
bulk manufacturer of the basic class(es) of controlled substance(s) 
listed.

     Dated: October 16, 2009.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. E9-25886 Filed 10-27-09; 8:45 am]

BILLING CODE 4410-09-P