[Federal Register Volume 60, Number 110 (Thursday, June 8, 1995)]
[Notices]
[Page 30319]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-13994]



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DEPARTMENT OF JUSTICE

Importation of Controlled Substances; Notice of Application

    Pursuant to Section 1008 of the Controlled Substances Import and 
Export Act (21 U.S.C. 958(i)), the Attorney General shall, prior to 
issuing a registration under this Section to a bulk manufacturer of a 
controlled substance in Schedule I or II and prior to issuing a 
regulation under Section 1002(a) authorizing the importation of such a 
substance, provide manufacturers holding registrations for the bulk 
manufacture of the substance an opportunity for a hearing.
    Therefore, in accordance with Section 1311.42 of Title 21, Code of 
Federal Regulations (CFR), notice is hereby given that on April 24, 
1995, Research Triangle Institute, Kenneth H. Davis, Jr., Hermann 
Building, East Institute Drive, P.O. Box 12194, Research Triangle Park, 
North Carolina 27709, made application to the Drug Enforcement 
Administration to be registered as an importer of the basic classes of 
controlled substances listed below:

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                           Drug                               Schedule  
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Marihuana (7360)..........................................  I           
Cocaine (9041)............................................  II          
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    The Institute plans to import the listed controlled substances to 
make Marihuana cigarettes and reference standards under the Institute's 
manufacturer registration.
    Any manufacturer holding, or applying for, registration as a bulk 
manufacturer of these basic classes of controlled substances may file 
written comments on or objections to the application described above 
and may, at the same time, file a written request for a hearing on such 
application in accordance with 21 CFR 1301.54 in such form as 
prescribed by 21 CFR 1216.47.
    Any such comments, objections, or requests for a hearing may be 
addressed to the Deputy Assistant Administrator, Office of Division 
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 (30 days from 
publication).
    This procedure is to be conducted simultaneously with and 
independent of the procedures described in 21 CFR 1311.42 (b), (c), 
(d), (e), and (f). As noted in a previous notice at 40 FR 43745-46 
(September 23, 1975), all applicants for registration to import basic 
classes of any controlled substances in Schedule I or II are and will 
continue to be required to demonstrate to the Deputy Assistant 
Administrator, Office of Division Control, Drug Enforcement 
Administration that the requirements for such registration pursuant to 
21 U.S.C. 958(a), 21 U.S.C. 823(a), and 21 CFR 1311.42 (a), (b), (c), 
(d), (e), and (f) are satisfied.

    Dated: May 30, 1995.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 95-13994 Filed 6-7-95; 8:45 am]
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