[Federal Register Volume 59, Number 94 (Tuesday, May 17, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-11922]
[[Page Unknown]]
[Federal Register: May 17, 1994]
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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 the 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 April 15,
1994, Research Biochemicals, Limited Partnership, One Strathmore Road,
Natick, Massachusetts 01760, 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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Methaqualone (2565)......................................... I
Ibnogaine (7260)............................................ I
Tetrahydrocannabinols (7370)................................ I
Bufotenine (7433)........................................... I
Dimethyltryptamine (7435)................................... I
Ethorphine (except HCl) (9056).............................. I
Methylphenidate (1724)...................................... II
Etorphine Hydrochloride (9059).............................. II
Diphenoxylate (9170)........................................ II
Metazocine (9240)........................................... II
Methadone (9250)............................................ II
Dextropropoxyphene, bulk (non-dosage forms) (9273).......... II
Fentanyl (9801)............................................. II
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The firms imports small amounts of controlled substances for
manufacturing into non-human reference standards.
Any manufacture 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 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 (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 a basic
class of any controlled substance 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 1311.42 (a), (b), (c),
(d) (e), and (f) are satisfied.
Dated: May 11, 1994.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control Drug
Enforcement Administration.
[FR Doc. 94-11922 Filed 5-16-94; 8:45 am]
BILLING CODE 4410-09-M
