Manufacturer of Controlled Substances; Notice of Registration, 10070 [2011-3924]

Download as PDF 10070 Federal Register / Vol. 76, No. 36 / Wednesday, February 23, 2011 / Notices Johnson Matthey Inc. to manufacture the listed basic classes of controlled substances is consistent with the public interest at this time. DEA has investigated Johnson Matthey 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: February 15, 2011. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. 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: February 16, 2011. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 2011–3924 Filed 2–22–11; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE Parole Commission [FR Doc. 2011–3925 Filed 2–22–11; 8:45 am] [5 U.S.C. Section 552b] BILLING CODE 4410–09–P Meetings; Sunshine Act; Public Announcement Pursuant to the Government in the Sunshine Act Public Law 94–409 DEPARTMENT OF JUSTICE Drug Enforcement Administration By Notice dated October 8, 2010, and published in the Federal Register on October 20, 2010, 75 FR 64745, Halo Pharmaceutical Inc., 30 North Jefferson Road, Whippany, New Jersey 07981, 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 mstockstill on DSKH9S0YB1PROD with NOTICES Dihydromorphine (9145) ............... Hydromorphone (9150) ................ I II Dihydromorphine is an intermediate in the manufacture of Hydromorphone and is not for commercial distribution. The company plans to manufacture Hydromorphone HCL for sale to other manufacturers and for the manufacture of other controlled substance dosage units for 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 Halo Pharmaceutical Inc. to manufacture the listed basic classes of controlled substances is consistent with the public interest at this time. DEA has investigated Halo Pharmaceutical Inc. to ensure that the company’s registration is consistent with the public interest. The VerDate Mar<15>2010 18:50 Feb 22, 2011 Jkt 223001 Dated: February 11, 2011. Isaac Fulwood, Chairman, U.S. Parole Commission. [FR Doc. 2011–3891 Filed 2–22–11; 8:45 am] Department of Justice, United States Parole Commission. DATE AND TIME: 10 a.m., Thursday, February 17, 2011. PLACE: U.S. Parole Commission, 5550 Friendship Boulevard, 4th Floor, Chevy Chase, Maryland 20815. STATUS: Closed. MATTERS CONSIDERED: The following matter will be considered during the closed meeting: Discussion of an original jurisdiction case pursuant to 28 CFR 2.17. AGENCY CONTACT: Patricia W. Moore, Staff Assistant to the Chairman, United States Parole Commission, (301) 492– 5933. AGENCY HOLDING MEETING: Manufacturer of Controlled Substances; Notice of Registration Drug Parole Commission, 5550 Friendship Boulevard, 4th Floor, Chevy Chase, Maryland 20815. The purpose of the meeting was to decide four petitions for reconsideration pursuant to 28 CFR Section 2.27 and one pursuant to 28 CFR Section 2.17. Four Commissioners were present, constituting a quorum when the vote to close the meeting was submitted. Public announcement further describing the subject matter of the meeting and certifications of General Counsel that this meeting may be closed by vote of the Commissioners present were submitted to the Commissioners prior to the conduct of any other business. Upon motion duly made, seconded, and carried, the following Commissioners voted that the meeting be closed: Isaac Fulwood, Cranston J. Mitchell, Patricia Cushwa and J. Patricia Wilson Smoot. In witness whereof, I make this official record of the vote taken to close this meeting and authorize this record to be made available to the public. Dated: February 15, 2011, Rockne Chickinell, General Counsel, U.S. Parole Commission. [FR Doc. 2011–3902 Filed 2–22–11; 8:45 am] BILLING CODE 4410–31–M DEPARTMENT OF JUSTICE United States Parole Commission Record of Vote of Meeting Closure (Pub. L. 94–409) (5 U.S.C. Sec. 552b) I, Isaac Fulwood, of the United States Parole Commission, was present at a meeting of said Commission, which started at approximately 11:30 a.m., on Thursday, February 10, 2011, at the U.S. PO 00000 Frm 00067 Fmt 4703 Sfmt 4703 BILLING CODE 4410–01–M DEPARTMENT OF LABOR Office of Workers’ Compensation Programs Division of Coal Mine Workers’ Compensation; Proposed Extension of Existing Collection; Comment Request ACTION: Notice. The Department of Labor, as part of its continuing effort to reduce paperwork and respondent burden, conducts a pre-clearance consultation program to provide the general public and Federal agencies with an opportunity to comment on proposed and/or continuing collections of information in accordance with the Paperwork Reduction Act of 1995 (PRA95) [44 U.S.C. 3506(c)(2)(A)]. This program helps to ensure that requested data can be provided in the desired format, reporting burden (time and financial resources) is minimized, collection instruments are clearly understood, and the impact of collection requirements on respondents can be properly assessed. Currently, the Office of Workers’ Compensation Programs is soliciting comments concerning its proposal to extend OMB approval of the information collection for the following medical reports: SUMMARY: E:\FR\FM\23FEN1.SGM 23FEN1

Agencies

[Federal Register Volume 76, Number 36 (Wednesday, February 23, 2011)]
[Notices]
[Page 10070]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-3924]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated October 8, 2010, and published in the Federal 
Register on October 20, 2010, 75 FR 64745, Halo Pharmaceutical Inc., 30 
North Jefferson Road, Whippany, New Jersey 07981, 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:

------------------------------------------------------------------------
                    Drug                               Schedule
------------------------------------------------------------------------
Dihydromorphine (9145).....................  I
Hydromorphone (9150).......................  II
------------------------------------------------------------------------

    Dihydromorphine is an intermediate in the manufacture of 
Hydromorphone and is not for commercial distribution. The company plans 
to manufacture Hydromorphone HCL for sale to other manufacturers and 
for the manufacture of other controlled substance dosage units for 
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 
Halo Pharmaceutical Inc. to manufacture the listed basic classes of 
controlled substances is consistent with the public interest at this 
time. DEA has investigated Halo Pharmaceutical 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: February 16, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 2011-3924 Filed 2-22-11; 8:45 am]
BILLING CODE 4410-09-P
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