Manufacturer of Controlled Substances, Notice of Registration, Chemica, 64144 [2012-25633]
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64144
Federal Register / Vol. 77, No. 202 / Thursday, October 18, 2012 / Notices
Drug
Schedule
Meperidine (9230) ........................
Methadone (9250) ........................
Methadone intermediate (9254) ...
Morphine (9300) ...........................
Oripavine (9330) ...........................
Thebaine (9333) ...........................
Opium tincture (9630) ..................
Opium, powdered (9639) .............
Opium, granulated (9640) ............
Oxymorphone (9652) ...................
Noroxymorphone (9668) ..............
Alfentanil (9737) ...........................
Remifentanil (9739) ......................
Sufentanil (9740) ..........................
Tapentadol (9780) ........................
Fentanyl (9801) ............................
II
II
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II
II
II
II
II
II
II
II
II
II
II
II
II
made application by renewal to the
Drug Enforcement Administration
(DEA) to be registered as a bulk
manufacturer of the basic classes of
controlled substances:
Drug
The company plans to manufacture
the listed controlled substances in bulk
for distribution and sale to its
customers. Regarding (9640) the
company plans to manufacture another
controlled substance for sale to its
customers.
No comments or objections have been
received. DEA has considered the
factors in 21 U.S.C. 823(a) and
determined that the registration of
Chattem Chemicals, Inc., to manufacture
the listed basic classes of controlled
substances is consistent with the public
interest at this time. DEA has
investigated Chattem Chemicals, Inc., to
ensure that the company’s registration is
consistent with the public interest. The
investigation has included inspection
and testing of the company’s physical
security systems, verification of the
company’s compliance with state and
local laws, and a review of the
company’s background and history.
Therefore, pursuant to 21 U.S.C. 823(a),
and in accordance with 21 CFR 1301.33,
the above named company is granted
registration as a bulk manufacturer of
the basic classes of controlled
substances listed.
Dated: October 9, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
Schedule
Tetrahydrocannabinols (7370) .....
3,4Methylenedioxymethamphetamine (MDMA) (7405).
Cocaine (9041) .............................
Oxycodone (9143) ........................
Hydrocodone (9193) .....................
Methadone (9250) ........................
Dextropropoxyphene, bulk (nondosage forms) (9273).
Morphine (9300) ...........................
I
I
II
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The company plans to manufacture
the listed controlled substances as bulk
reagents for use in drug abuse testing.
No comments or objections have been
received. DEA has considered the
factors in 21 U.S.C. 823(a) and
determined that the registration of Lin
Zhi International, Inc., to manufacture
the listed basic classes of controlled
substances is consistent with the public
interest at this time. DEA has
investigated Lin Zhi International Inc.,
to ensure that the company’s
registration is consistent with the public
interest. The investigation has included
inspection and testing of the company’s
physical security systems, verification
of the company’s compliance with state
and local laws, and a review of the
company’s background and history.
Therefore, pursuant to 21 U.S.C. 823,
and in accordance with 21 CFR 1301.33,
the above named company is granted
registration as a bulk manufacturer of
the basic classes of controlled
substances listed.
Dated: October 9, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. 2012–25635 Filed 10–17–12; 8:45 am]
BILLING CODE 4410–09–P
[FR Doc. 2012–25637 Filed 10–17–12; 8:45 am]
Drug Enforcement Administration
DEPARTMENT OF JUSTICE
Manufacturer of Controlled
Substances, Notice of Registration,
Chemica
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Drug Enforcement Administration
Manufacturer of Controlled
Substances; Notice of Registration;
Lin Zhi International, Inc.
By Notice dated May 15, 2012, and
published in the Federal Register on
May 22, 2012, 77 FR 30326, Lin Zhi
International, Inc., 670 Almanor
Avenue, Sunnyvale, California 94085,
VerDate Mar<15>2010
18:15 Oct 17, 2012
Jkt 229001
By Notice dated June 18, 2012, and
published in the Federal Register on
June 26, 2012, 77 FR 38086, Chemica,
316 West 130th Street, Los Angeles,
California 90061, made application by
renewal to the Drug Enforcement
Administration (DEA) to be registered as
a bulk manufacturer of
PO 00000
Frm 00050
Fmt 4703
Sfmt 4703
Dated: October 9, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. 2012–25633 Filed 10–17–12; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF LABOR
Mine Safety and Health Administration
Affirmative Decisions on Petitions for
Modification Granted in Whole or in
Part
Mine Safety and Health
Administration (MSHA), Labor.
ACTION: Notice.
AGENCY:
DEPARTMENT OF JUSTICE
BILLING CODE 4410–09–P
Methamphetamine (1105), a basic class
of controlled substance listed in
schedule II.
The above listed controlled substance
is an intermediate in the manufacture of
Benzphetamine, a schedule III nonnarcotic controlled substance. The
methamphetamine will not be sold as a
commercial product. The company
plans to utilize a bulk active
pharmaceutical ingredient (API), as an
intermediate for the development of
another controlled substance, and
further distribution to its customers.
No comments or objections have been
received. DEA has considered the
factors in 21 U.S.C. 823(a), and
determined that the registration of
Chemica to manufacture the listed basic
class of controlled substance is
consistent with the public interest at
this time. DEA has investigated Chemica
to ensure that the company’s
registration is consistent with the public
interest. The investigation has included
inspection and testing of the company’s
physical security systems, verification
of the company’s compliance with state
and local laws, and a review of the
company’s background and history.
Therefore, pursuant to 21 U.S.C. 823,
and in accordance with 21 CFR 1301.33,
the above named company is granted
registration as a bulk manufacturer of
the basic class of controlled substance
listed.
Section 101(c) of the Federal
Mine Safety and Health Act of 1977 and
30 CFR part 44 govern the application,
processing, and disposition of petitions
for modification. This Federal Register
Notice notifies the public that MSHA
has investigated and issued a final
decision on certain mine operator
petitions to modify a safety standard.
ADDRESSES: Copies of the final decisions
are posted on MSHA’s Web Site at
https://www.msha.gov/indexes/
SUMMARY:
E:\FR\FM\18OCN1.SGM
18OCN1
Agencies
[Federal Register Volume 77, Number 202 (Thursday, October 18, 2012)]
[Notices]
[Page 64144]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-25633]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances, Notice of Registration,
Chemica
By Notice dated June 18, 2012, and published in the Federal
Register on June 26, 2012, 77 FR 38086, Chemica, 316 West 130th Street,
Los Angeles, California 90061, made application by renewal to the Drug
Enforcement Administration (DEA) to be registered as a bulk
manufacturer of Methamphetamine (1105), a basic class of controlled
substance listed in schedule II.
The above listed controlled substance is an intermediate in the
manufacture of Benzphetamine, a schedule III non-narcotic controlled
substance. The methamphetamine will not be sold as a commercial
product. The company plans to utilize a bulk active pharmaceutical
ingredient (API), as an intermediate for the development of another
controlled substance, and further distribution to its customers.
No comments or objections have been received. DEA has considered
the factors in 21 U.S.C. 823(a), and determined that the registration
of Chemica to manufacture the listed basic class of controlled
substance is consistent with the public interest at this time. DEA has
investigated Chemica to ensure that the company's registration is
consistent with the public interest. The investigation has included
inspection and testing of the company's physical security systems,
verification of the company's compliance with state and local laws, and
a review of the company's background and history.
Therefore, pursuant to 21 U.S.C. 823, and in accordance with 21 CFR
1301.33, the above named company is granted registration as a bulk
manufacturer of the basic class of controlled substance listed.
Dated: October 9, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2012-25633 Filed 10-17-12; 8:45 am]
BILLING CODE 4410-09-P