Withdrawal of Approval of New Animal Drug Applications; Phenylbutazone; Pyrantel; Tylosin; Sulfamethazine; Correction, 22713 [2011-9778]

Download as PDF 22713 Federal Register / Vol. 76, No. 78 / Friday, April 22, 2011 / Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request Title: Developmental Disabilities Annual Protection and Advocacy Systems Program Performance Report. OMB No.: 0980–0160. Description: This information collection is required by Federal statute. Each State Protection and Advocacy System must prepare and submit a program Performance Report for the preceding fiscal year of activities and accomplishments and of conditions in the State. The information in the Annual Report will be aggregated into a national profile of Protection and Advocacy Systems. It will also provide the Administration on Developmental Disabilities (ADD) with an overview of program trends and achievements and will enable ADD to respond to administration and congressional requests for specific information on program activities. This information will also be used to submit a Centennial Report to Congress as well as to comply with requirements in the Government Performance and Results Act of 1993. Respondents: Protection and Advocacy Entities. ANNUAL BURDEN ESTIMATES Instrument Number of respondents Number of responses per respondent Average burden hours per response Total burden hours Program Performance Report ......................................................................... 57 1 44 2,508 Estimated Total Annual Burden Hours: 2,508. Additional Information: Copies of the proposed collection may be obtained by writing to the Administration for Children and Families, Office of Administration, Office of Information Services, 370 L’Enfant Promenade, SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. All requests should be identified by the title of the information collection. E-mail address: infocollection@acf.hhs.gov. OMB Comment: OMB is required to make a decision concerning the collection of information between 30 and 60 days after publication of this document in the Federal Register. Therefore, a comment is best assured of having its full effect if OMB receives it within 30 days of publication. Written comments and recommendations for the proposed information collection should be sent directly to the following: Office of Management and Budget, Paperwork Reduction Project, Fax: 202–395–7285, E-mail: OIRA_SUBMISSION@OMB.EOP.GOV, Attn: Desk Officer for the Administration for Children and Families. Robert Sargis, Reports Clearance Officer. [FR Doc. 2011–9772 Filed 4–21–11; 8:45 am] mstockstill on DSKH9S0YB1PROD with NOTICES BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration Health Resources and Services Administration [Docket No. FDA–2011–N–0033] Withdrawal of Approval of New Animal Drug Applications; Phenylbutazone; Pyrantel; Tylosin; Sulfamethazine; Correction AGENCY: Food and Drug Administration, HHS. ACTION: Notice; correction. The Food and Drug Administration (FDA) published a document in the Federal Register of March 2, 2011 (76 FR 11490), providing notice of the voluntary withdrawal of approval of eight new animal drug applications (NADAs). That document contained an error in the preamble. FDA is correcting the name and address for the sponsor of five of the NADAs. This correction is being made to improve the accuracy of the Federal Register. FOR FURTHER INFORMATION CONTACT: George K. Haibel, Center for Veterinary Medicine (HFV–6), Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 240–276–9019, e-mail: george.haibel@fda.hhs.gov. SUPPLEMENTARY INFORMATION: In the Federal Register of March 2, 2011, in FR Doc. 2011–4545, on page 11490, in the first column, correct the Truow Nutrition, Inc., name and address to read: Trouw Nutrition USA LLC, P.O. Box 219, 115 Executive Dr., Highland, IL 62249. SUMMARY: Dated: April 15, 2011. Bernadette Dunham, Director, Center for Veterinary Medicine. [FR Doc. 2011–9778 Filed 4–21–11; 8:45 am] BILLING CODE 4160–01–P VerDate Mar<15>2010 16:01 Apr 21, 2011 Jkt 223001 PO 00000 Frm 00047 Fmt 4703 Sfmt 4703 Administration for Children and Families Advisory Committee on the Maternal, Infant and Early Childhood Home Visiting Program Evaluation; Notice of Meeting In accordance with section 10(a)(2) of the Federal Advisory Committee Act (Pub. L. 92–463, 5 U.S.C. appendix 2), notice is hereby given of the following meeting: Name: Advisory Committee on the Maternal, Infant and Early Childhood Home Visiting (MIECHV) Program Evaluation. Date and Time: Thursday, May 5, 2011: 9 a.m.–5:15 p.m. EST. Friday, May 6, 2011: 9 a.m.–2:15 p.m. EST. Place: Hilton Alexandria Old Town, 1767 King Street, Alexandria, Virginia 22314. (703) 837–0440. This notice announces a forthcoming meeting of a public advisory committee of the Health Resources and Services Administration and the Administration for Children and Families. The meeting will be open to the public. This notice is being published less than 15 days prior to the meeting due to difficulties in securing adequate and accessible space to accommodate the public. Meeting Registration: To register for the meeting, the public can contact Carolyn Swaney at cswaney@icfi.com. Agenda: The purpose of this meeting is to gather comments from the Committee on the design of the MIECHV E:\FR\FM\22APN1.SGM 22APN1

Agencies

[Federal Register Volume 76, Number 78 (Friday, April 22, 2011)]
[Notices]
[Page 22713]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-9778]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2011-N-0033]


Withdrawal of Approval of New Animal Drug Applications; 
Phenylbutazone; Pyrantel; Tylosin; Sulfamethazine; Correction

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice; correction.

-----------------------------------------------------------------------

SUMMARY: The Food and Drug Administration (FDA) published a document in 
the Federal Register of March 2, 2011 (76 FR 11490), providing notice 
of the voluntary withdrawal of approval of eight new animal drug 
applications (NADAs). That document contained an error in the preamble. 
FDA is correcting the name and address for the sponsor of five of the 
NADAs. This correction is being made to improve the accuracy of the 
Federal Register.

FOR FURTHER INFORMATION CONTACT: George K. Haibel, Center for 
Veterinary Medicine (HFV-6), Food and Drug Administration, 7519 
Standish Pl., Rockville, MD 20855, 240-276-9019, e-mail: 
george.haibel@fda.hhs.gov.

SUPPLEMENTARY INFORMATION: In the Federal Register of March 2, 2011, in 
FR Doc. 2011-4545, on page 11490, in the first column, correct the 
Truow Nutrition, Inc., name and address to read: Trouw Nutrition USA 
LLC, P.O. Box 219, 115 Executive Dr., Highland, IL 62249.

    Dated: April 15, 2011.
Bernadette Dunham,
Director, Center for Veterinary Medicine.
[FR Doc. 2011-9778 Filed 4-21-11; 8:45 am]
BILLING CODE 4160-01-P
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