[Federal Register Volume 68, Number 231 (Tuesday, December 2, 2003)]
[Notices]
[Page 67480]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 03-29970]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances, Notice of Registration

    By Notice dated July 22, 2003, and published in the Federal 
Register on August 5, 2003, (68 FR 46227), Wildlife Laboratories, Inc., 
1401 Duff Drive, Suite 600, Fort Collins, Colorado 80524, made 
application by renewal to the Drug Enforcement Administration for 
registration as a bulk manufacturer of Carfentanil (9743), a basic 
class of controlled substance listed in Schedule II.
    The firm plans to manufacture the listed controlled substance for 
distribution to its customers.
    No comments or objections have been received. DEA has considered 
the factors in title 21, United States Code, section 823(a) and 
determined that the registration of Wildlife Laboratories, Inc. to 
manufacture the listed controlled substances 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. This 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 28 CFR 0.100 and 0.104, the Deputy Assistant 
Administrator, Office of Diversion Control, hereby orders that the 
application submitted by the above firm for registration as a bulk 
manufacturer of the basic class of controlled substance listed is 
granted.

    Dated: November 14, 2003.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 03-29970 Filed 12-1-03; 8:45 am]
BILLING CODE 4410-09-M