[Federal Register Volume 77, Number 226 (Friday, November 23, 2012)]
[Notices]
[Page 70188]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2012-28493]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Application;
Alltech Associates, Inc.
Pursuant to Sec. 1301.33(a), Title 21 of the Code of Federal
Regulations (CFR), this is notice that on September 14, 2012, Alltech
Associates Inc., 2051 Waukegan Road, Deerfield, Illinois 60015, made
application to the Drug Enforcement Administration (DEA) to be
registered as a bulk manufacturer of the following basic classes of
controlled substances:
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Drug Schedule
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2C-T-2 (2-(4-Ethylthio-2,5- I
dimethoxyphenyl)ethanamine) (7385).
2C-1 (2-(4-lodo-2,5-dimethoxyphenyl) I
Ethanamine) (7518).
2C-C (2-(4-Chloro-2,5-dimethoxyphenyl) I
ethanamine (7519).
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The company plans to manufacture high purity drug standards used
for analytical applications only in clinical, toxicological, and
forensic laboratories.
Any other such applicant, and any person who is presently
registered with DEA to manufacture such substances, may file comments
or objections to the issuance of the proposed registration pursuant to
21 CFR 1301.33(a).
Any such comments or objections should be addressed, in
quintuplicate, to the Drug Enforcement Administration, Office of
Diversion Control, Federal Register Representative (ODL), 8701
Morrissette Drive, Springfield, Virginia 22152; and must be filed no
later than January 22, 2013.
Dated: November 14, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2012-28493 Filed 11-21-12; 8:45 am]
BILLING CODE 4410-09-P