Manufacturer of Controlled Substances; Notice of Registration; Boehringer Ingelheim Chemicals, Inc.; Correction, 151 [2013-31362]

Download as PDF Federal Register / Vol. 79, No. 1 / Thursday, January 2, 2014 / Notices 151 DEPARTMENT OF JUSTICE Drug Enforcement Administration Drug Enforcement Administration Importer of Controlled Substances; Notice of Application; Hospira maindgalligan on DSK5TPTVN1PROD with NOTICES DEPARTMENT OF JUSTICE Manufacturer of Controlled Substances; Notice of Application; American Radiolabeled Chemicals, Inc. Dated: December 16, 2013. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 2013–31362 Filed 12–31–13; 8:45 am] Pursuant to 21 CFR 1301.34(a), this is notice that on September 25, 2013, Hospira, 1776 North Centennial Drive, McPherson, Kansas 67460–1247, made application by renewal to the Drug Enforcement Administration (DEA) for registration 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. Any bulk manufacturer who is presently, or is applying to be, registered with DEA to manufacture such basic class of controlled substance 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 (ODW), 8701 Morrissette Drive, Springfield, Virginia 22152; and must be filed no later than February 3, 2014. 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 schedules 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 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: December 16, 2013. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 2013–31364 Filed 12–31–13; 8:45 am] Pursuant to 21 CFR 1301.33(a), this is notice that on October 24, 2013, American Radiolabeled Chemicals, Inc., 101 Arc Drive, St. Louis, Missouri 63146, made application by written correspondence to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of Methadone (9250), a basic class of controlled substance in schedule II. The company plans to manufacture small quantities of the listed controlled substance as radiolabeled compounds for biochemical research. Any other such applicant, and any person who is presently registered with DEA to manufacture such substance, may file comments or objections to the issuance of the proposed registration pursuant to 21 CFR 1301.33(a). Any such written comments or objections should be addressed, in quintuplicate, to the Drug Enforcement Administration, Office of Diversion Control, Federal Register Representative (ODW), 8701 Morrissette Drive, Springfield, Virginia 22152; and must be filed no later than March 3, 2014. Dated: December 16, 2013. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 2013–31363 Filed 12–31–13; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Registration; Boehringer Ingelheim Chemicals, Inc.; Correction In Federal Register (FR DOC) 2013– 25096 on page 64019, in the issue of Friday, October 25, 2013, make the following corrections: On page 64019, in the first column, in the table, the first cell inadvertently omitted basic class of controlled substance Amphetamine (1100), and the second column, in the table, the last cells should read ‘‘II’’. BILLING CODE 4410–09–P VerDate Mar<15>2010 17:20 Dec 31, 2013 Jkt 232001 PO 00000 Frm 00060 Fmt 4703 Sfmt 4703 BILLING CODE 4410–09–P NATIONAL ARCHIVES AND RECORDS ADMINISTRATION [NARA–2014–013] Records Schedules; Availability and Request for Comments National Archives and Records Administration (NARA). ACTION: Notice of availability of proposed records schedules; request for comments. AGENCY: The National Archives and Records Administration (NARA) publishes notice at least once monthly of certain Federal agency requests for records disposition authority (records schedules). Once approved by NARA, records schedules provide mandatory instructions on what happens to records when no longer needed for current Government business. They authorize the preservation of records of continuing value in the National Archives of the United States and the destruction, after a specified period, of records lacking administrative, legal, research, or other value. Notice is published for records schedules in which agencies propose to destroy records not previously authorized for disposal or reduce the retention period of records already authorized for disposal. NARA invites public comments on such records schedules, as required by 44 U.S.C. 3303a(a). DATES: Requests for copies must be received in writing on or before February 3, 2014. Once the appraisal of the records is completed, NARA will send a copy of the schedule. NARA staff usually prepares appraisal memorandums that contain additional information concerning the records covered by a proposed schedule. These, too, may be requested and will be provided once the appraisal is completed. Requesters will be given 30 days to submit comments. ADDRESSES: You may request a copy of any records schedule identified in this notice by contacting Records Management Services (ACNR) using one of the following means: Mail: NARA (ACNR), 8601 Adelphi Road, College Park, MD 20740–6001. Email: request.schedule@nara.gov. FAX: 301–837–3698. SUMMARY: E:\FR\FM\02JAN1.SGM 02JAN1

Agencies

[Federal Register Volume 79, Number 1 (Thursday, January 2, 2014)]
[Notices]
[Page 151]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-31362]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration; 
Boehringer Ingelheim Chemicals, Inc.; Correction

    In Federal Register (FR DOC) 2013-25096 on page 64019, in the issue 
of Friday, October 25, 2013, make the following corrections:
    On page 64019, in the first column, in the table, the first cell 
inadvertently omitted basic class of controlled substance Amphetamine 
(1100), and the second column, in the table, the last cells should read 
``II''.

    Dated: December 16, 2013.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 2013-31362 Filed 12-31-13; 8:45 am]
BILLING CODE 4410-09-P

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