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

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Manufacturers Notice of Application - 2009

FR Doc E9-25893[Federal Register: October 28, 2009 (Volume 74, Number 207)] [Notices] [Page 55588] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr28oc09-112]


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 April 9, 2009, Aldrich Chemical Company Inc., DBA Isotec, 3858 Benner Road, Miamisburg, Ohio 45342-4304, made application by renewal to the Drug Enforcement Administration (DEA) as a bulk manufacturer of the basic classes of controlled substances listed in schedules I and II:

Drug Schedule
Gamma Hydroxybutyric Acid (2010)  I
Methaqualone (2565)  I
Ibogaine (7260)  I
Tetrahydrocannabinols (7370)  I
2,5-Dimethoxyamphetamine (7396)  I
Psilocyn (7438)  I
Normorphine (9313)  I
Acetylmethadol (9601)  I
Alphacetylmethadol except levo-alphacetylmethadol (9603)  I
Normethadone (9635)  I
Norpipanone (9636)  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-Piperidinocyclohexane-carbonitrile (8603)  II
Cocaine (9041)  II
Codeine (9050)  II
Oxycodone (9143)  II
Hydromorphone (9150)  II
Benzoylecgonine (9180)  II
Ethylmorphine (9190)  II
Hydrocodone (9193)  II
Isomethadone (9226)  II
Meperidine (9230)  II
Meperidine intermediate-A (9232)  II
Meperidine intermediate-B (9233)  II
Methadone (9250)  II
Methadone intermediate (9254)  II
Dextropropoxyphene, bulk, (non-dosage forms) (9273)  II
Morphine (9300)  II
Thebaine (9333)  II
Levo-alphacetylmethadol (9648)  II
Oxymorphone (9652)  II

The company plans to manufacture small quantities of the listed controlled substances to produce isotope labeled standards for drug testing and analysis.

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 pursuant to 21 CFR 1301.33(a).

Any such written comments or objections should be addressed, in quintuplicate, to the Drug Enforcement Administration, Office of Diversion Control, Federal Register Representative (ODL), 8701 Morrissette Drive, Springfield, Virginia 22152; and must be filed no later than December 28, 2009.

Dated: October 20, 2009.

Joseph T. Rannazzisi, 
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.

[FR Doc. E9-25893 Filed 10-27-09; 8:45 am]

BILLING CODE 4410-09-M

 

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

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U.S. DEPARTMENT OF JUSTICE  •  DRUG ENFORCEMENT ADMINISTRATION
Diversion Control Division  •  8701 Morrissette Drive  •  Springfield, VA 22152  •  1-800-882-9539

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