[Federal Register Volume 60, Number 49 (Tuesday, March 14, 1995)]
[Notices]
[Page 13734]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-6218]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated November 21, 1994, and published in the Federal
Register on November 29, 1994, (59 FR 61002), Isotec, Inc., 3858 Benner
Road, Miamisburg, Ohio 45342, made application to the Drug Enforcement
Administration (DEA) to be registered as a bulk manufacturer of the
basic classes of controlled substances listed below:
------------------------------------------------------------------------
Drug Schedule
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Cathinone (1235).......................................... I
Methcathinone (1237)...................................... I
N-Ethylamphetamine (1475)................................. I
N,N-Dimethylamphetamine (1480)............................ I
Aminorex (1585)........................................... I
Methaqualone (2565)....................................... I
Lysergic acid diethylamide (7315)......................... I
Tetrahydrocannabinols (7370).............................. I
Mescaline (7381).......................................... I
2,5-Dimethoxyamphetamine (7396)........................... I
3,4-Methylenedioxyamphetamine (7400)...................... I
3,4-Methylenedioxy-N-ethylamphetamine (7404).............. I
3,4-Methylenedioxymeth- Pamphetamine (7405)............... I
4-Methoxyamphetamine (7411)............................... I
N-Ethyl-1-phenylcyclohexylamine (7455).................... I
Dihydromorphine (9145).................................... I
Normorphine (9313)........................................ I
Acetylmethadol (9601)..................................... I
Alphacetylmethadol Except Levo-Alphacetylmethadol (9603).. I
Normethadone (9635)....................................... I
3-Methylfentanyl (9813)................................... I
Amphetamine (1100)........................................ II
Methamphetamine (1105).................................... II
Methylphenidate (1724).................................... II
Amobarbital (2125)........................................ II
Pentobarbital (2270)...................................... II
Secobarbital (2315)....................................... II
1-Phenylcyclohexylamine (7460)............................ II
Phencyclidine (7471)...................................... II
Phenylacetone (8501)...................................... II
1-Piperidinocyclohexanecar- Pbonitrile (8603)............. II
Codeine (9050)............................................ II
Dihydrocodeine (9120)..................................... II
Oxycodone (9143).......................................... II
Hydromorphone (9150)...................................... II
Benzoylecgonine (9180).................................... II
Ethylmorphine (9190)...................................... II
Hydrocodone (9193)........................................ II
Isomethadone (9226)....................................... II
Meperidine (9230)......................................... II
Methadone (9250).......................................... II
Methadone intermediate (9254)............................. II
Dextropropoxyphene, bulk (non-dosage forms) (9273)........ II
Morphine (9300)........................................... II
Levo-Alphacetylmethadol (9648)............................ II
Oxymorphone (9652)........................................ II
Fentanyl (9801)........................................... II
------------------------------------------------------------------------
Comments were filed by two registered manufacturers. The comments
were considered, however, DEA determined that the application should be
approved. Therefore, pursuant to Section 303 of the Comprehensive Drug
Abuse Prevention and Control Act of 1970 and Title 21, Code of Federal
Regulations, Deputy Assistant Administrator, Office of Diversin
Control, 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 above is approved and registration is granted.
Dated: March 8, 1995.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 95-6218 Filed 3-13-95; 8:45 am]
BILLING CODE 4410-09-M
