[Federal Register Volume 71, Number 14 (Monday, January 23, 2006)]
[Notices]
[Page 3545]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: E6-719]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

    Pursuant to Sec.  1301.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on August 31, 2005, Clariant LSM 
(Missouri), Inc., 2460 W. Bennett Street (or P.O. Box 1246, Zip: 
65801), Springfield, Missouri 65807-1229, made application by letter to 
the Drug Enforcement Administration (DEA) for registration as a bulk 
manufacturer of Phenylacetone (8501), and Methadone Intermediate 
(9254), a basic class of controlled substances listed in Schedule II.
    The company plans to manufacture in bulk, for sale to its 
customers.
    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 written comments or objections being sent via regular mail 
may be addressed, in quintuplicate, to the Deputy Assistant 
Administrator, Office of Diversion Control, Drug Enforcement 
Administration, Washington, DC 20537, Attention: DEA Federal Register 
Representative, Liaison and Policy Section (ODL); or any being sent via 
express mail should be sent to DEA Headquarters, Attention: DEA Federal 
Register Representative/ODL, 2401 Jefferson-Davis Highway, Alexandria, 
Virginia 22301; and must be filed no later than March 24, 2006.

    Dated: January 11, 2006.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. E6-719 Filed 1-20-06; 8:45 am]
BILLING CODE 4410-09-P