Manufacturer of Controlled Substances Notice of Registration, 72976 [2011-30546]
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72976
Federal Register / Vol. 76, No. 228 / Monday, November 28, 2011 / Notices
Drug
Schedule
Noroxymorphone (9668) ..............................................................................................................................................................................
The company plans to manufacture
high purity drug standards used for
analytical applications only in clinical,
toxicological, and forensic laboratories.
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
Alltech Associates, Inc. to manufacture
the listed basic classes of controlled
substances is consistent with the public
interest at this time. DEA has
investigated Alltech Associates 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: November 18, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
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,
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.
[FR Doc. 2011–30543 Filed 11–25–11; 8:45 am]
Dated: November 18, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
BILLING CODE 4410–09–P
II
for sale to its customers for formulation
into finished pharmaceuticals.
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
Boehringer Ingelheim Chemicals, Inc.,
to manufacture the listed basic classes
of controlled substances is consistent
with the public interest at this time.
DEA has investigated Boehringer
Ingelheim 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: November 18, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. 2011–30546 Filed 11–25–11; 8:45 am]
[FR Doc. 2011–30549 Filed 11–25–11; 8:45 am]
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DEPARTMENT OF JUSTICE
DEPARTMENT OF JUSTICE
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Drug Enforcement Administration
Manufacturer of Controlled
Substances Notice of Registration
Drug Enforcement Administration
Manufacturer of Controlled
Substances Notice of Registration
By Notice dated June 14, 2011, and
published in the Federal Register on
June 22, 2011, 76 FR 36577, Chattem
Chemicals Inc., 3801 St. Elmo Avenue,
Chattanooga, Tennessee 37409, made
application by letter to the Drug
Enforcement Administration (DEA) to
be registered as a bulk manufacturer of
the following basic classes of controlled
substances:
Drug
Manufacturer of Controlled
Substances; Notice of Registration
By Notice dated June 13, 2011, and
published in the Federal Register on
June 22, 2011, 76 FR 36577, Boehringer
Ingelheim Chemicals, Inc., 2820 N.
Normandy Drive, Petersburg, Virginia
23805–9372, made application by
renewal to the Drug Enforcement
Administration (DEA) to be registered as
a bulk manufacturer of the following
basic classes of controlled substances:
Schedule
pmangrum on DSK3VPTVN1PROD with NOTICES
Drug
Gamma
Hydroxybutyric
Acid
(2010).
Opium tincture (9630) ..................
Opium, powdered (9639) .............
Opium, granulated (9640) ............
Tapentadol (9780) ........................
Amphetamine (1100) ....................
Lisdexamfetamine (1205) .............
Methylphenidate (1724) ................
Methadone (9250) ........................
Methadone intermediate (9254) ...
II
II
II
II
The company plans to manufacture
the listed controlled substances in bulk
VerDate Mar<15>2010
15:34 Nov 25, 2011
Schedule
I
Jkt 226001
II
II
II
II
II
The company plans to manufacture
the listed controlled substances in bulk
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By Notice dated June 22, 2011, and
published in the Federal Register on
June 29, 2011, 76 FR 38209, Pharmagra
Labs Inc., 158 McLean Road, Brevard,
North Carolina 28712, made application
to the Drug Enforcement Administration
(DEA) to be registered as a bulk
manufacturer of Pentobarbital (2270), a
basic class of controlled substance in
schedule II.
The company plans to manufacture
the listed controlled substance for
analytical research and clinical trials.
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
Pharmagra Labs, Inc. to manufacture the
listed basic class of controlled substance
is consistent with the public interest at
this time. DEA has investigated
Pharmagra Labs, Inc. to ensure that the
E:\FR\FM\28NON1.SGM
28NON1
Agencies
[Federal Register Volume 76, Number 228 (Monday, November 28, 2011)]
[Notices]
[Page 72976]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-30546]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances Notice of Registration
By Notice dated June 14, 2011, and published in the Federal
Register on June 22, 2011, 76 FR 36577, Chattem Chemicals Inc., 3801
St. Elmo Avenue, Chattanooga, Tennessee 37409, made application by
letter to the Drug Enforcement Administration (DEA) to be registered as
a bulk manufacturer of the following basic classes of controlled
substances:
------------------------------------------------------------------------
Drug Schedule
------------------------------------------------------------------------
Gamma Hydroxybutyric Acid (2010)........... I
Opium tincture (9630)...................... II
Opium, powdered (9639)..................... II
Opium, granulated (9640)................... II
Tapentadol (9780).......................... II
------------------------------------------------------------------------
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, 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: November 18, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2011-30546 Filed 11-25-11; 8:45 am]
BILLING CODE 4410-09-P