[Federal Register Volume 69, Number 217 (Wednesday, November 10, 2004)]
[Notices]
[Page 65229]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 04-25103]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated May 21, 2004, and published in the Federal Register 
on June 3, 2004, (69 FR 31411), American Radiolabeled Chemicals, Inc., 
101 Arc Drive, St. Louis, Missouri 63146, made application by renewal 
to the Drug Enforcement Administration (DEA) for registration as a bulk 
manufacturer of the basic classes of controlled substances listed 
below:

------------------------------------------------------------------------
                    Drug                               Schedule
------------------------------------------------------------------------
Gamma hydroxybutyric acid (2010)...........  I
Dimethyltryptamine (7435)..................  I
Dihydromorphine (9145).....................  I
Cocaine (9041).............................  II
Codeine (9050).............................  II
Hydromorphone (9150).......................  II
Benzoylecgonine (9180).....................  II
Ecgonine (9180)............................  II
Meperidine (9230)..........................  II
Metazocine (9240)..........................  II
Morphine (9300)............................  II
Oxymorphone (9652).........................  II
------------------------------------------------------------------------

    The company plans to manufacture in bulk, small quantities of the 
listed controlled substances as radiolabeled compounds.
    No comments or objections have been received. DEA has considered 
the factors in 21 U.S.C. 823(a) and determined that the registration of 
American Radiolabeled Chemicals, Inc. to manufacture the listed basic 
classes of controlled substances is consistent with the public interest 
at this time. DEA has investigated American Radiolabeled Chemicals, 
Inc. to ensure that the company's registration is consistent with the 
public interest. The 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 in accordance with 21 CFR 1301.33, the above named company is 
granted registration as a bulk manufacturer of the basic classes of 
controlled substances listed.

    Dated: November 1, 2004.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 04-25103 Filed 11-9-04; 8:45 am]
BILLING CODE 4410-09-P