Bulk Manufacturer of Controlled Substances Application: AUSTIN PHARMA, LLC, 34554 [2014-14144]

Download as PDF 34554 Federal Register / Vol. 79, No. 116 / Tuesday, June 17, 2014 / Notices DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–392] Bulk Manufacturer of Controlled Substances Application: AUSTIN PHARMA, LLC ACTION: Notice of Correction. In Federal Register document (FR DOC) 2014–12944, on page 32322, in the issue of Wednesday, June 4, 2014, make the following correction: On page 32322, in the second column, the third paragraph, the first sentence should read as follows: In reference to drug code 7360, the company plans to manufacture synthetic cannabidiol in bulk for sale to its customers. Dated: June 10, 2014. Joseph T. Rannazzisi, Deputy Assistant Administrator. the DEA Office of Diversion Control (‘‘Deputy Assistant Administrator’’) pursuant to sec. 7(g) of 28 CFR pt. 0, subpt. R, App. In accordance with 21 CFR 1301.33(a), this is notice that on February 5, 2014, Euticals, Inc., 2460 W. Bennett Street, Springfield, Missouri 65807–1229, applied to be registered as a bulk manufacturer of the following basic classes of controlled substances: Controlled substance Methadone (9250) ........................ Oripavine (9330) ........................... Schedule II II The company plans to manufacture the listed controlled substances in bulk for distribution and sale to its customers. Dated: June 10, 2014. Joseph T. Rannazzisi, Deputy Assistant Administrator. [FR Doc. 2014–14124 Filed 6–16–14; 8:45 am] BILLING CODE 4410–09–P [FR Doc. 2014–14144 Filed 6–16–14; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF LABOR DEPARTMENT OF JUSTICE [Docket No. DEA–392] Bulk Manufacturer of Controlled Substances Application: Euticals, Inc. ACTION: Notice of Application. Registered bulk manufacturers of the affected basic classes, and applicants therefore, may file written comments on or objections to the issuance of the proposed registration in accordance with 21 CFR 1301.33(a) on or before August 18, 2014. ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/ODW, 8701 Morrissette Drive, Springfield, Virginia 22152. The Attorney General has delegated his authority under the Controlled Substances Act to the Administrator of the Drug Enforcement Administration (DEA), 28 CFR 0.100(b). Authority to exercise all necessary functions with respect to the promulgation and implementation of 21 CFR part 1301, incident to the registration of manufacturers, distributors, and dispensers of controlled substances (other than final orders in connection with suspension, denial, or revocation of registration) has been redelegated to the Deputy Assistant Administrator of tkelley on DSK3SPTVN1PROD with NOTICES VerDate Mar<15>2010 16:43 Jun 16, 2014 Jkt 232001 Agency Information Collection Activities; Submission for OMB Review; Comment Request; Records of Tests and Examinations of Mine Personnel Hoisting Equipment ACTION: DATES: SUPPLEMENTARY INFORMATION: Authority: 44 U.S.C. 3507(a)(1)(D). Notice. The Department of Labor (DOL) is submitting the Mine Safety and Health Administration (MSHA) sponsored information collection request (ICR) titled, ‘‘Records of Tests and Examinations of Mine Personnel Hoisting Equipment,’’ to the Office of Management and Budget (OMB) for review and approval for continued use, without change, in accordance with the Paperwork Reduction Act of 1995 (PRA), 44 U.S.C. 3501 et seq. Public comments on the ICR are invited. DATES: The OMB will consider all written comments that agency receives on or before July 17, 2014. ADDRESSES: A copy of this ICR with applicable supporting documentation; including a description of the likely respondents, proposed frequency of response, and estimated total burden may be obtained free of charge from the RegInfo.gov Web site at http:// www.reginfo.gov/public/do/ PRAViewICR?ref_nbr=201403-1219-003 (this link will only become active on the day following publication of this notice) or by contacting Michel Smyth by telephone at 202–693–4129, TTY 202– SUMMARY: PO 00000 Frm 00069 Fmt 4703 Sfmt 4703 This ICR seeks to extend PRA authority for the Records of Tests and Examinations of Mine Personnel Hoisting Equipment information collection. Various MSHA regulations make it mandatory for a covered mine operator to make and maintain records of specific tests and inspections of mine personnel hoisting systems, including wire ropes, to ensure each system remains safe to operate while in use. Mine Safety and Health Act of 1977 section 103(h) authorizes this information collection. See 30 U.S.C. 813(h). This information collection is subject to the PRA. A Federal agency generally cannot conduct or sponsor a collection of information, and the public is generally not required to respond to an information collection, unless it is approved by the OMB under the PRA and displays a currently valid OMB Control Number. In addition, notwithstanding any other provisions of law, no person shall generally be subject to penalty for failing to comply with a collection of information that does not display a valid Control Number. See 5 CFR 1320.5(a) and 1320.6. The DOL obtains OMB approval for this information collection under Control Number 1219–0034. OMB authorization for an ICR cannot be for more than three (3) years without renewal, and the current approval for this collection is scheduled to expire on July 31, 2014. The DOL seeks to extend PRA authorization for this information SUPPLEMENTARY INFORMATION: Office of the Secretary Drug Enforcement Administration 693–8064, (these are not toll-free numbers) or by email at DOL_PRA_ PUBLIC@dol.gov. Submit comments about this request by mail or courier to the Office of Information and Regulatory Affairs, Attn: OMB Desk Officer for DOL– MSHA, Office of Management and Budget, Room 10235, 725 17th Street NW., Washington, DC 20503; by Fax: 202–395–6881 (this is not a toll-free number); or by email: OIRA_ submission@omb.eop.gov. Commenters are encouraged, but not required, to send a courtesy copy of any comments by mail or courier to the U.S. Department of Labor-OASAM, Office of the Chief Information Officer, Attn: Departmental Information Compliance Management Program, Room N1301, 200 Constitution Avenue NW., Washington, DC 20210; or by email: DOL_PRA_PUBLIC@dol.gov. FOR FURTHER INFORMATION CONTACT: Contact Michel Smyth by telephone at 202–693–4129, TTY 202–693–8064, (these are not toll-free numbers) or by email at DOL_PRA_PUBLIC@dol.gov. E:\FR\FM\17JNN1.SGM 17JNN1

Agencies

[Federal Register Volume 79, Number 116 (Tuesday, June 17, 2014)]
[Notices]
[Page 34554]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-14144]



[[Page 34554]]

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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Bulk Manufacturer of Controlled Substances Application: AUSTIN 
PHARMA, LLC

ACTION: Notice of Correction.

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    In Federal Register document (FR DOC) 2014-12944, on page 32322, in 
the issue of Wednesday, June 4, 2014, make the following correction:
    On page 32322, in the second column, the third paragraph, the first 
sentence should read as follows:
    In reference to drug code 7360, the company plans to manufacture 
synthetic cannabidiol in bulk for sale to its customers.

    Dated: June 10, 2014.
Joseph T. Rannazzisi,
Deputy Assistant Administrator.
[FR Doc. 2014-14144 Filed 6-16-14; 8:45 am]
BILLING CODE 4410-09-P