[Federal Register Volume 62, Number 132 (Thursday, July 10, 1997)]
[Notices]
[Page 37077]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 97-18104]
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DEPARTMENT OF JUSTICE
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 May 29, 1997, Applied Science
Labs, Division of Alltech Associates, Inc., 2701 Carolean Industrial
Drive, P.O. Box 440, State College, Pennsylvania 16801, made
application to the Drug Enforcement Administration (DEA) for
registration as a bulk manufacturer of the basic classes of controlled
substances listed below:
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Drug Schedule
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Methcathinone (1237)......................... I
N-Ethylamphetamine (1475).................... I
N, N-Dimethylamphetamine (1480).............. I
4-Methylaminorex (cis isomer) (1590)......... I
Lysergic acid diethylamide (7315)............ I
Mescaline (7381)............................. I
3, 4-Methylenedioxyamphetamine (7400)........ I
N-Hydroxy-3, 4-methylenedioxy- amphetamine I
(7402).
3, 4-Methylenedioxy-N-ethyl- amphetamine I
(7404).
3, 4-Methylenedioxymeth- amphetamine (7405).. I
N-Ethyl-1-phenylcyclohexylamine (7455)....... I
1-(1-Phenylcyclohexyl) pyrrolidine (7458).... I
1-[1- (2-Thienyl) cyclohexyl]- piperidine I
(7470).
Dihydromorphine (9145)....................... I
Phenylcyclohexylamine (7460)................. II
Phencyclidine (7471)......................... II
Phenylacetone (8501)......................... II
1-Piperidinocyclohexane- carbonitrile (PCC) II
(8603).
Cocaine (9041)............................... II
Codeine (9050)............................... II
Dihydrocodeine (9120)........................ II
Benzoylecgonine (9180)....................... II
Morphine (9300).............................. II
Oxymorphone (9652)........................... II
Noroxymorphone (9668)........................ II
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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 Diversion Control,
Drug Enforcement Administration, United States Department of Justice,
Washington, D.C. 20537, Attention: DEA Federal Register Representative
(CCR), and must be filed no later than September 8, 1997.
Dated: June 23, 1997.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 97-18104 Filed 7-9-97; 8:45 am]
BILLING CODE 4410-09-M