Diversion Control Division, US Department of Justice, Drug Enforcement Administration

Manufacturers Notice of Application - 2004

FR Doc 04-3475 [Federal Register: February 18, 2004 (Volume 69, Number 32)] [Notices] [Page 7655] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr18fe04-61]


Drug Enforcement Administration

Manufacturer of Controlled Substances; Notice of Application

Pursuant to section 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on October 23, 2003, Applied Science Labs, Division of Alltech Associates Inc., 2701 Carolean Industrial Drive, P.O. Box 440, State College, Pennsylvania 16801, made application by letter to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of the basic class of controlled substances listed below:

Drug  Schedule 
2, 5-dimethoxy-4-(n)-propylthiophenethylaminie (2C-T-7) (7348) I
Alpha-methyltryptamine (AMT) (7432) I
5-methoxy-N-, N-diisopropyltryptamine (5-MeO-DIPT) (7439) I

The firm plans to manufacture small quantities of the listed controlled substances for reference standards. 

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. 

Any such comments or objections may be addressed, in quintuplicate, to the Deputy Assistant Administrator, Office of Division Control, Drug Enforcement Administration, United States Department of Justice, Washington, DC 20537, Attention: Federal Register Representative, Office of Chief Counsel (CCD) and must be filed no later than April 19, 2004.

Dated: February 4, 2004. 

Laura M. Nagel, 
Deputy Assistant Administrator, Office of Diversion Control. 

[FR Doc. 04-3475 Filed 2-17-04; 8:45 am]


NOTICE: This is an unofficial version. An official version of this publication may be obtained directly from the Government Publishing Office (GPO).

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