[Federal Register: December 1, 2006 (Volume 71, Number 231)]
[Notices]               
[Page 69591]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr01de06-106]                         

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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

 
Importer of Controlled Substances; Notice of Application

    Pursuant to 21 U.S.C. Sec.  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 21 U.S.C. 952(a)(2)(B) 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 21 CFR 1301.34(a), this is notice 
that on October 3, 2006, JFC Technologies LLC., 100 West Main Street, 
P.O. Box 669, Bound Brook, NJ 08805, made application by renewal to the 
Drug Enforcement Administration (DEA) to be registered as an importer 
of Meperidine intermediate-B (9233), a basic class of controlled 
substance listed in schedule II.
    The company plans to import the basic class of controlled substance 
for the production of controlled substances for distribution to its 
customers.
    Any manufacturer who is presently, or is applying to be, registered 
with DEA to manufacture such basic class of controlled substance may 
file comments or objections to the issuance of the proposed 
registration and may, at the same time, file a written request for a 
hearing on such application pursuant to 21 CFR 1301.43 and in such form 
as prescribed by 21 CFR 1316.47.
    Any such written comments or objections being sent via regular mail 
should be addressed, in quintuplicate, to the Deputy Assistant 
Administrator, Office of Diversion Control, Drug Enforcement 
Administration, Washington, DC 20537, Attention: DEA Federal Register 
Representative/ODL; or any being sent via express mail should be sent 
to DEA Headquarters, Attention: DEA Federal Register Representative/
ODL, 2401 Jefferson-Davis Highway, Alexandria, VA 22301; and must be 
filed no later than January 2, 2007.
    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 published in the Federal 
Register on September 23, 1975, (40 FR 43745-46), all applicants for 
registration to import a basic class of any controlled substance listed 
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. Sec.  958(a), 21 U.S.C. 823(a), 
and 21 CFR 1301.34(b), (c), (d), (e) and (f) are satisfied.

    Dated: November 21, 2006.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
 [FR Doc. E6-20346 Filed 11-30-06; 8:45 am]

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