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

Manufacturers Notice of Application - 2003

[Federal Register: June 19, 2003 (Volume 68, Number 118)] [Notices] [Page 36844] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr19jn03-86]


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 July 23, 2001, and April 21, 2003, Eli-Elsohly Laboratories, Inc., Mahmoud A. Elsohly Ph.D., 5 Industrial Park Drive, Oxford, Mississippi 38655, made application by renewal to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of the basic classes of Schedule I and II controlled substances listed below:

Drug Schedule
Tetrahydrocannabinols (7370) I
Dihydromorphine (9145) I
Amphetamine (1100) II
Methamphetamine (1105) II
Cocaine (9041) II
Codeine (9050) II
Dihydrocodeine (9120) II
Oxycodone (9143) II
Hydromorphone (9150) II
Benzoylecognine (9180) II
Hydrocodone (9193) II
Morphine (9300) II

The firm plans to manufacture non-deuterated controlled substances for use as analytical standards and deuterated controlled substances for use as internal 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 Diversion Control, Drug Enforcement Administration, United States Department of Justice, Washington, DC 20537, Attention: DEA Federal Register Representative (CCD) and must be filed no later than August 18, 2003.

Dated: June 6, 2003.

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

[FR Doc. 03-15536 Filed 6-18-03; 8:45 am]

BILLING CODE 4410-09-M

 

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