[Federal Register: October 29, 2003 (Volume 68, Number 209)]
[Notices]
[Page 61699]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr29oc03-59]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By notice dated June 6, 2003, and published in the Federal Register
on June 19, 2003, (68 FR 36844), 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 to be registered as a bulk manufacturer of the basic
classes of Schedules I and II controlled substances listed below:
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Drug Schedule
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Tetrahydrocannabinols (7370)............... I
Dihydromorphine (9145)..................... I
Codeine (9050)............................. II
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
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The firm plans to manufacture non-deuterated controlled substances
for use as analytical standards and deuterated controlled substances
for use as internal standards.
No comments or objections have been received. DEA has considered
the factors in title 21, United States Code, section 823(a) and
determined that the registration of Eli-Elsohly Laboratories, Inc. to
manufacture the listed controlled substances is consistent with the
public interest at this time. DEA has investigated Eli-Elsohly
Laboratories, Inc. to ensure that the company's registration is
consistent with the public interest. This 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 28 CFR 0.100 and 0.104, the Deputy Assistant
Administrator, Office of Diversion Control, hereby orders that the
application submitted by the above firm for registration as a bulk
manufacturer of the basic classes of controlled substances listed is
granted.
Dated: October 15, 2003.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 03-27243 Filed 10-28-03; 8:45 am]
BILLING CODE 4410-09-M