[Federal Register Volume 64, Number 100 (Tuesday, May 25, 1999)]
[Notices]
[Pages 28215-28216]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 99-13098]
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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 Sec. 1311.42 of Title 21, Code of
Federal Regulations (CFR), notice is hereby given that on January 25,
1999, Sigma Chemical Company, Subsidiary of Sigma-Aldrich Company, 3500
Dekalb Street, St. Louis, Missouri 63118, made application by renewal
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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Cathinone (1235)........................... I
Methcathinone (1237)....................... I
Methaqualone (2565)........................ I
Ibogaine (7260)............................ I
Lysergic acid diethylamide (7315).......... I
Tetrahydrocannabinols (7370)............... I
Mescaline (7381)........................... I
4-Bromo-2,5-dimethoxyamphetamine (7391).... I
3, 4-Methylenedioxyamphetamine (7400)...... I
3, 4-Methylenedioxy-N-ethylamphetamine I
(7404).
3, 4-Methylenedioxymethamphetamine (7405).. I
4-Methoxyamphetamine (7411)................ I
Psilocyn (7438)............................ I
Heroin (9200).............................. I
Normorphine (9313)......................... I
Etonitazene (9624)......................... I
Amphetamine (1100)......................... II
Methamphetamine (1105)..................... II
Methylphenidate (1724)..................... II
Amobarbital (2125)......................... II
Pentobarbital (2270)....................... II
Secobarbital (2315)........................ II
Phencyclidine (7471)....................... II
Cocaine (9041)............................. II
Codeine (9050)............................. II
Oxycodone (9143)........................... II
Hydromorphone (9150)....................... II
Benzoylecogonine (9180).................... II
Ethylmorphine (9190)....................... II
Hydrocodone (9193)......................... II
Levorphanol (9220)......................... II
Meperidine (9230).......................... II
Methadone (9250)........................... II
Dextropropoxyphene, bulk, (non-dosage II
forms) (9273).
Morphine (9300)............................ II
Thebaine (9333)............................ II
Opium powdered (9639)...................... II
Oxymorphone (9652)......................... II
Fentanyl (9802)............................ II
------------------------------------------------------------------------
The firm plans to repackage and offer as pure standards controlled
substances in small milligram quantities for drug testing and analysis.
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
[[Page 28216]]
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, in quintuplicate, 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
June 24, 1999.
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 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: May 14, 1999.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 99-13098 Filed 5-24-99; 8:45 am]
BILLING CODE 4410-09-M