98-18215. Importation of Controlled Substances; Notice of Application  

  • [Federal Register Volume 63, Number 131 (Thursday, July 9, 1998)]
    [Notices]
    [Pages 37140-37141]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 98-18215]
    
    
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    DEPARTMENT OF JUSTICE
    
    Drug Enforcement Administration
    
    
    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 1301.34 of Title 21, Code of 
    Federal Regulations (CFR), notice is hereby given that on March 31, 
    1998, Research Triangle Institute, Kenneth H. Davis, Jr., Hermann 
    Building, East Institute Drive, P.O. Box 12194, Research Triangle Park, 
    North Carolina 27709, made application by renewal to the Drug 
    Enforcement Administration to be registered as an importer of the basic 
    classes of controlled substances listed below:
    
    ------------------------------------------------------------------------
                        Drug                               Schedule         
    ------------------------------------------------------------------------
    Marihuana (7360)...........................  I                          
    Cocaine (9041).............................  II                         
    ------------------------------------------------------------------------
    
        The firm plans to import small quantities of the listed controlled 
    substances for the National Institute of Drug Abuse and other clients.
        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 1301.43 in such form as 
    prescribed by 21 CFR 1316.47.
        Any such comments, objections or requests for a hearing may be 
    addressed, in quintuplicate, to the Deputy Assistant Administrator, 
    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 
    August 10, 1998.
        This procedure is to be conducted simultaneously with and 
    independent of the procedures described in 21 CFR 1301.34(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 the 
    basic classes
    
    [[Page 37141]]
    
    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 Diversion 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 1301.34(a), (b), (c), (d), (e), and (f) are 
    satisfied.
    
        Dated: June 10, 1998.
    John H. King,
    Deputy Assistant Administrator, Office of Diversion Control, Drug 
    Enforcement Administration.
    [FR Doc. 98-18215 Filed 7-8-98; 8:45 am]
    BILLING CODE 4410-09-M
    
    
    

Document Information

Published:
07/09/1998
Department:
Drug Enforcement Administration
Entry Type:
Notice
Document Number:
98-18215
Pages:
37140-37141 (2 pages)
PDF File:
98-18215.pdf