[Federal Register: October 13, 1999 (Volume 64, Number 197)]
[Notices]               
[Page 55487-55488]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr13oc99-78]                         

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DEPARTMENT OF JUSTICE

Drug enforcement Administration

 
Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated July 16, 1999, and published in the Federal 
Register on July 29, 1999, (63 FR 40542), American Radiolabeled 
Chemical, Inc., 11624 Bowling Green Drive, St. Louis, Missouri 63146, 
made application by

[[Page 55488]]

letter to the Drug Enforcement Administration (DEA) to be registered as 
a bulk manufacturer of the basic classes of controlled substances 
listed below:

------------------------------------------------------------------------
                    Drug                               Schedule
------------------------------------------------------------------------
Dimethyltryptamine (7435)..................  I
Dihydromorphine (9145).....................  I
Cocaine (9041).............................  II
Codeine (9050).............................  II
Benzoylecgonine (9180).....................  II
Meperidine (9230)..........................  II
Metazocine (9240)..........................  II
Morphine (9300)............................  II
Oxymorphone (9652).........................  II
------------------------------------------------------------------------

    The firm plans to bulk manufacture small quantities of the listed 
controlled substances as radiolabeled compounds.
    No comments or objections have been received. DEA has considered 
the factors in Title 21, United States Code, Section 823(a) and 
determined that the registration of American Radiolabeled Chemical, 
Inc. to manufacture the listed controlled substances is consistent with 
the public interest at this time. DEA has investigated American 
Radiolabeled Chemical, Inc. on a regular basis to ensure that the 
company's continued registration is consistent with the public 
interest. These investigations have included inspection and testing of 
the company's physical security systems, audits of the company's 
records, 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 28 CFR 0.100 and 0.104, the Deputy 
Assistant Administrator, Office of Diversion Control, hereby orders 
that application submitted by the above firm for registration as a bulk 
manufacturer of the basic classes of controlled substances listed above 
is granted.

    Dated: October 1, 19999.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control Drug 
Enforcement Administration.
[FR Doc. 99-26599 Filed 10-12-99; 8:45 am]
BILLING CODE 4410-09-M