[Federal Register Volume 74, Number 207 (Wednesday, October 28, 2009)]
[Notices]
[Page 55585]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: E9-25891]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated April 17, 2009, and published in the Federal 
Register on April 29, 2009, (74 FR 19598), Archimica, Inc., 2460 W. 
Bennett Street, Springfield, Missouri 65807-1229, made application by 
letter to the Drug Enforcement Administration (DEA) to be registered as 
a bulk manufacturer of Lisdexamfetamine (1205), a basic class of 
controlled substance listed in schedule II.
    The company plans to manufacture the controlled substance in bulk 
for distribution to its customers.
    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 
Archimica, Inc. to manufacture the listed basic classes of controlled 
substances is consistent with the public interest at this time. DEA has 
investigated Archimica, 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 classes of controlled substances listed.

    Dated: October 20, 2009.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. E9-25891 Filed 10-27-09; 8:45 am]
BILLING CODE 4410-09-P