[Federal Register Volume 62, Number 91 (Monday, May 12, 1997)]
[Notices]
[Page 25974]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 97-12301]



[[Page 25974]]

-----------------------------------------------------------------------

DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Importation of Controlled Substances; 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 Sec. 1311.42 of Title 21, Code of 
Federal Regulations (CFR), notice is hereby given that on March 17, 
1997, Roche Diagnostic Systems, Inc., 1080 U.S. Highway 202, 
Somerville, New Jersey 08876-3771, made application by renewal to the 
Drug Enforcement Administration to be registered as an importer of 
tetrahydrocannabinols (7370), a basic class of controlled substance 
listed in Schedule I.
    The tetrahydrocannabinols will be utilized exclusively for non-
human consumption in drug of abuse detection kits.
    Any manufacturer holding, or applying for, registration as a bulk 
manufacturer of this basic class of controlled substance 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 1316.47.
    Any such comments, objections, or requests for a hearing may be 
addressed to the Acting Deputy Assistant Administrator, Office of 
Diversion Control, Drug Enforcement Administration, United States 
Department of Justice, Washington, DC 20537, Attention: DEA Federal 
Register Representative (CCR), and must be filed no later than June 11, 
1997.
    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 a basic 
class of any controlled substance in Schedule I or II are and will 
continue to be required to demonstrate to the Acting 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 1311.42 (a), (b), (c), 
(d), (e), and (f) are satisfied.

    Dated: April 2, 1997.
Terrance W. Woodworth,
Acting Deputy Assistant Administrator, Office of Diversion Control, 
Drug Enforcement Administration.
[FR Doc. 97-12301 Filed 5-9-97; 8:45 am]
BILLING CODE 4410-09-M