Sunshine Act Meeting, 12621 [2012-5183]

Download as PDF Federal Register / Vol. 77, No. 41 / Thursday, March 1, 2012 / Notices 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 21 U.S.C. 952(a)(2) 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 21 CFR 1301.34(a), this is notice that on December 30, 2011, Mylan Pharmaceuticals, Inc., 781 Chestnut Ridge Road, Morgantown, West Virginia 26505, made application by letter to the Drug Enforcement Administration (DEA) to be registered as an importer of the following basic classes of controlled substances: Drug Schedule mstockstill on DSK4VPTVN1PROD with NOTICES Amphetamine (1100) .................... Methadone (9250) ........................ Morphine (9300) ........................... II II II The company plans to import the listed controlled substances in finished dosage form (FDF) from foreign sources for analytical testing and clinical trials in which the foreign FDF will be compared to the company’s own domestically-manufactured FDF. This analysis is required to allow the company to export domesticallymanufactured FDF to foreign markets. Any bulk manufacturer who is presently, or is applying to be, registered with DEA to manufacture such basic classes of controlled substances may file comments or objections to the issuance of the proposed registration and may, at the same time, file a written request for a hearing on such application pursuant to 21 CFR 1301.43, and in such form as prescribed by 21 CFR 1316.47. Any such written comments or objections should be addressed, in quintuplicate, to the Drug Enforcement Administration, Office of Diversion Control, Federal Register Representative (ODL), 8701 Morrissette Drive, Springfield, Virginia 22152; and must be filed no later than April 2, 2012. 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 published in the Federal Register on September 23, 1975, 40 FR 43745–46, all applicants for registration to import a basic class of any controlled substance 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 VerDate Mar<15>2010 17:25 Feb 29, 2012 Jkt 226001 for such registration pursuant to 21 U.S.C. 958(a); 21 U.S.C. 823(a); and 21 CFR 1301.34(b), (c), (d), (e), and (f) are satisfied. Dated: February 23, 2012. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. 12621 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. [FR Doc. 2012–4992 Filed 2–29–12; 8:45 am] Dated: February 23, 2012. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. BILLING CODE 4410–09–P [FR Doc. 2012–4994 Filed 2–29–12; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE Drug Enforcement Administration Importer of Controlled Substances; Notice of Registration; Mylan Pharmaceuticals Inc. By Notice dated December 22, 2011, and published in the Federal Register on December 29, 2011, 76 FR 81978, Mylan Pharmaceuticals, Inc., 781 Chestnut Ridge Road, Morgantown, West Virginia 26505, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as an importer of the following basic classes of controlled substances: Drug Schedule Methylphenidate (1724) ................ Oxycodone (9143) ........................ Hydromorphone (9150) ................ Fentanyl (9801) ............................ II II II II The company plans to import the listed controlled substances in finished dosage form (FDF) from foreign sources for analytical testing and clinical trials in which the foreign FDF will be compared to the company’s own domestically-manufactured FDF. This analysis is required to allow the company to export domesticallymanufactured FDF to foreign markets. 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 Mylan Pharmaceuticals, 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 Mylan Pharmaceuticals, 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) PO 00000 Frm 00069 Fmt 4703 Sfmt 4703 DEPARTMENT OF JUSTICE Parole Commission Sunshine Act Meeting 1:30 p.m., Thursday, March 8, 2012. PLACE: U.S. Parole Commission, 90 K Street NE., 3rd Floor, Washington, DC. STATUS: Closed. MATTERS TO BE CONSIDERED: Consideration of two original jurisdiction cases pursuant to 28 CFR 2.27. TIME AND DATE: CONTACT PERSON FOR MORE INFORMATION: Patricia W. Moore, Staff Assistant to the Chairman, U.S. Parole Commission, 90 K Street NE., 3rd Floor, Washington, DC 20530, (202) 346–7001. Dated: February 27, 2012. Rockne Chickinell, General Counsel, U.S. Parole Commission. [FR Doc. 2012–5183 Filed 2–28–12; 4:15 pm] BILLING CODE 4410–31–P MISSISSIPPI RIVER COMMISSION Sunshine Act Meetings Agency Holding the Meetings: Mississippi River Commission. AGENCY: Time and Date: 9 a.m., March 26, 2012. Place: On board MISSISSIPPI V at River Park, Tiptonville, TN. Status: Open to the public. Matters To Be Considered: (1) Summary report by President of the Commission on national and regional issues affecting the U.S. Army Corps of Engineers and Commission programs and projects on the Mississippi River and its tributaries; (2) District Commander’s overview of current project issues within the Memphis District; and (3) Presentations by local organizations and members of the public giving views or comments on any issue affecting the programs or projects of the Commission and the Corps of Engineers. DATES: E:\FR\FM\01MRN1.SGM 01MRN1

Agencies

[Federal Register Volume 77, Number 41 (Thursday, March 1, 2012)]
[Notices]
[Page 12621]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-5183]


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DEPARTMENT OF JUSTICE

Parole Commission


Sunshine Act Meeting

TIME AND DATE: 1:30 p.m., Thursday, March 8, 2012.

PLACE: U.S. Parole Commission, 90 K Street NE., 3rd Floor, Washington, 
DC.

STATUS: Closed.

MATTERS TO BE CONSIDERED: Consideration of two original jurisdiction 
cases pursuant to 28 CFR 2.27.

CONTACT PERSON FOR MORE INFORMATION: Patricia W. Moore, Staff Assistant 
to the Chairman, U.S. Parole Commission, 90 K Street NE., 3rd Floor, 
Washington, DC 20530, (202) 346-7001.

    Dated: February 27, 2012.
Rockne Chickinell,
General Counsel, U.S. Parole Commission.
[FR Doc. 2012-5183 Filed 2-28-12; 4:15 pm]
BILLING CODE 4410-31-P

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