Importer of Controlled Substances; Notice of Registration, 17967 [2011-7537]
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17967
Federal Register / Vol. 76, No. 62 / Thursday, March 31, 2011 / Notices
By order of the Commission:
Issued: March 28, 2011.
William R. Bishop,
Hearings and Meetings Coordinator.
Drug Enforcement Administration
Importer of Controlled Substances;
Notice of Registration
[FR Doc. 2011–7671 Filed 3–29–11; 11:15 am]
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JOINT BOARD FOR THE
ENROLLMENT OF ACTUARIES
Meeting of the Advisory Committee;
Meeting
Joint Board for the Enrollment
of Actuaries.
AGENCY:
Notice of Federal Advisory
Committee meeting.
ACTION:
The Executive Director of the
Joint Board for the Enrollment of
Actuaries gives notice of a closed
meeting of the Advisory Committee on
Actuarial Examinations.
SUMMARY:
The meeting will be held on
April 29, 2011, from 8:30 a.m. to 5 p.m.
DATES:
The meeting will be held at
Mercer, 4400 Comerica Bank Tower,
1717 Main Street, Dallas, TX 75201.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Patrick W. McDonough, Executive
Director of the Joint Board for the
Enrollment of Actuaries, 202–622–8225.
Notice is
hereby given that the Advisory
Committee on Actuarial Examinations
will meet at Mercer, 4400 Comerica
Bank Tower, 1717 Main Street, Dallas,
TX, on April 29, 2011, from 8:30 a.m.
to 5 p.m.
The purpose of the meeting is to
discuss topics and questions that may
be recommended for inclusion on future
Joint Board examinations in actuarial
mathematics, pension law and
methodology referred to in 29 U.S.C.
1242(a)(1)(B).
A determination has been made as
required by section 10(d) of the Federal
Advisory Committee Act, 5 U.S.C. App.,
that the subject of the meeting falls
within the exception to the open
meeting requirement set forth in Title 5
U.S.C. 552b(c)(9)(B), and that the public
interest requires that such meeting be
closed to public participation.
wwoods2 on DSK1DXX6B1PROD with NOTICES
SUPPLEMENTARY INFORMATION:
Dated: March 25, 2011.
Patrick W. McDonough,
Executive Director, Joint Board for the
Enrollment of Actuaries.
[FR Doc. 2011–7518 Filed 3–30–11; 8:45 am]
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11:23 Mar 31, 2011
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the following basic classes of controlled
substances:
DEPARTMENT OF JUSTICE
By Notice dated October 8, 2010, and
published in the Federal Register on
October 20, 2010 75 FR 64744, Hospira
Inc., 1776 North Centennial Drive,
McPherson, Kansas 67460–1247, made
application by renewal to the Drug
Enforcement Administration (DEA) to
be registered as an importer of
Remifentanil (9739), a basic class of
controlled substance listed in schedule
II.
The company plans to import
Remifentanil for use in dosage form
manufacturing.
No comments or objections have been
received. DEA has considered the
factors in 21 U.S.C. 823(a) and 952(a),
and determined that the registration of
Hospira Inc. to import the basic class of
controlled substance is consistent with
the public interest, and with United
States obligations under international
treaties, conventions, or protocols in
effect on May 1, 1971, at this time. DEA
has investigated Hospira 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. 952(a)
and 958(a), and in accordance with 21
CFR 1301.34, the above named company
is granted registration as an importer of
the basic class of controlled substance
listed.
Dated: March 21, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
Drug
Raw Opium (9600) .......................
Concentrate of Poppy Straw
(9670).
Schedule
II
II
The company plans to import narcotic
raw materials for manufacturing and
further distribution to its customers.
The company is registered with DEA as
a manufacturer of several controlled
substances that are manufactured from
raw opium, poppy straw, and
concentrate of poppy straw.
No comments or objections have been
received. DEA has considered the
factors in 21 U.S.C. 823(a) and 952(a)
and determined that the registration of
Cody Laboratories, Inc. to import the
basic classes of controlled substances is
consistent with the public interest, and
with United States obligations under
international treaties, conventions, or
protocols in effect on May 1, 1971. DEA
has investigated Cody Laboratories, 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. 952(a)
and 958(a), and in accordance with 21
CFR 1301.34, the above named company
is granted registration as an importer of
the basic classes of controlled
substances listed.
Dated: March 21, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. 2011–7542 Filed 3–30–11; 8:45 am]
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[FR Doc. 2011–7537 Filed 3–30–11; 8:45 am]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Importer of Controlled Substances;
Notice of Registration
By Notice dated October 19, 2010, and
published in the Federal Register on
October 26, 2010, 75 FR 65658, Cody
Laboratories Inc., 601 Yellowstone
Avenue, Cody, Wyoming 82414–3921,
made application by renewal to the
Drug Enforcement Administration
(DEA) to be registered as an importer of
PO 00000
Frm 00151
Fmt 4703
Sfmt 4703
Importer of Controlled Substances;
Notice of Registration
By Notice dated November 19, 2010,
and published in the Federal Register
on December 3, 2010 75 FR 75494,
Mylan Technologies, Inc., 110 Lake
Street, Saint Albans, Vermont 05478,
made application by renewal to the
Drug Enforcement Administration
(DEA) to be registered as an importer of
the following basic classes of controlled
substances:
E:\FR\FM\31MR1.SGM
31MR1
Agencies
[Federal Register Volume 76, Number 62 (Thursday, March 31, 2011)]
[Notices]
[Page 17967]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-7537]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Importer of Controlled Substances; Notice of Registration
By Notice dated October 8, 2010, and published in the Federal
Register on October 20, 2010 75 FR 64744, Hospira Inc., 1776 North
Centennial Drive, McPherson, Kansas 67460-1247, made application by
renewal to the Drug Enforcement Administration (DEA) to be registered
as an importer of Remifentanil (9739), a basic class of controlled
substance listed in schedule II.
The company plans to import Remifentanil for use in dosage form
manufacturing.
No comments or objections have been received. DEA has considered
the factors in 21 U.S.C. 823(a) and 952(a), and determined that the
registration of Hospira Inc. to import the basic class of controlled
substance is consistent with the public interest, and with United
States obligations under international treaties, conventions, or
protocols in effect on May 1, 1971, at this time. DEA has investigated
Hospira 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.
952(a) and 958(a), and in accordance with 21 CFR 1301.34, the above
named company is granted registration as an importer of the basic class
of controlled substance listed.
Dated: March 21, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2011-7537 Filed 3-30-11; 8:45 am]
BILLING CODE 4410-09-P