[Federal Register: August 22, 2006 (Volume 71, Number 162)]
[Notices]               
[Page 48944-48945]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr22au06-79]                         

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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 25, 2006, American 
Radiolabeled Chemicals, Inc., 101 Arc Drive, St. Louis, Missouri 63146, 
made application by renewal, and by correspondence dated June 2, 2006, 
to the Drug Enforcement Administration (DEA) for registration as a bulk 
manufacturer of the basic classes of controlled substances listed in 
Schedules I and II:

[[Page 48945]]



------------------------------------------------------------------------
                    Drug                               Schedule
------------------------------------------------------------------------
Gamma hydroxybutyric acid (2010)............  I
Ibogaine (7260).............................  I
Lysergic acid diethylamide (7315)...........  I
Tetrahydrocannabinols (7370)................  I
Dimethyltryptamine (7435)...................  I
Dihydromorphine (9145)......................  I
Amphetamine (1100)..........................  II
Methamphetamine (1105)......................  II
Amobarbital (2125)..........................  II
Phencyclidine (7471)........................  II
Phenylacetone (8501)........................  II
Cocaine (9041)..............................  II
Codeine (9050)..............................  II
Dihydrocodeine(9120)........................  II
Oxycodone (9143)............................  II
Hydromorphone (9150)........................  II
Ecgonine (9180).............................  II
Hydrocodone (9193)..........................  II
Meperidine (9230)...........................  II
Metazocine (9240)...........................  II
Morphine (9300).............................  II
Thebaine (9333).............................  II
Oxymorphone (9652)..........................  II
Fentanyl (9801).............................  II
------------------------------------------------------------------------

    The company plans to manufacture small quantities of the listed 
controlled substances as radiolabeled compounds for biochemical 
research.
    Any other such applicant and any person who is presently registered 
with DEA to manufacture such a substance 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 being sent via regular mail 
should be addressed, in quintuplicate, to the Deputy Assistant 
Administrator, Office of Diversion Control, Drug Enforcement 
Administration, Washington, DC 20537, Attention: DEA Federal Register 
Representative/ODL; or any being sent via express mail should be sent 
to DEA Headquarters, Attention: DEA Federal Register Representative/
ODL, 2401 Jefferson-Davis Highway, Alexandria, Virginia 22301; and must 
be filed no later than October 23, 2006.

     Dated: August 15, 2006.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. E6-13840 Filed 8-21-06; 8:45 am]

BILLING CODE 4410-09-P