[Federal Register Volume 65, Number 164 (Wednesday, August 23, 2000)]
[Notices]
[Pages 51331-51332]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 00-21486]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Application

    Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on June 15, 2000, Radian 
International LLC, 14050 Summit Drive #121, P.O. Box 201088, Austin, 
Texas 78720-1088, made application by letter to the Drug Enforcement 
Administration (DEA) for registration as a bulk manufacturer of the 
basic classes of controlled substances listed below:

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                    Drug                               Schedule
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Gamma hydroxybutyric acid (2010)...........  I
Thebaine (9333)............................  II
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    The firm plans to manufacture small quantities of the listed 
controlled substances to make deuterated and non-deuterated drug 
reference standards which will be distributed to analytical and 
forensic laboratories for drug testing programs.
    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.
    Any such comments or objections may be addressed, in quintuplicate, 
to the Deputy Assistant Administrator,

[[Page 51332]]

Office of Diversion Control, Drug Enforcement Administration, United 
States Department of Justice, Washington, D.C. 20537, Attention: DEA 
Federal Register Representative (CCR), and must be filed no later than 
October 23, 2000.

    Dated: August 8, 2000.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 00-21486 Filed 8-22-00; 8:45 am]
BILLING CODE 4410-09-M