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19488 Federal Register / Vol. 70, No.

70 / Wednesday, April 13, 2005 / Notices

will be sent to all grantees after the elsewhere in this issue of the Federal committees and, therefore, encourages
awards are made. Register, FDA is amending the animal nominations of qualified candidates
drug regulations to remove portions from these groups.
VII. Agency Contacts
reflecting approval of this NADA. DATES: Nominations will be accepted for
Program Office Contact: Katherine DATES: Withdrawal of approval is current vacancies and for those that will
Gray, U.S. Department of Health and effective April 25, 2005. or may occur through December 31,
Human Services, Administration for FOR FURTHER INFORMATION CONTACT: 2005. Because vacancies occur on
Children and Families, ACYF—Head Pamela K. Esposito, Center for various dates throughout the year, there
Start Bureau, 330 C Street SW., Switzer Veterinary Medicine (HFV–212), Food is no cutoff date for the receipt of
Room 2211, Washington, DC 20447, and Drug Administration, 7519 Standish nominations.
Phone: 312–353–2260, E-mail: Pl., Rockville, MD 20855, 301–827–
kgray@acf.hhs.gov. ADDRESSES: All nominations should be
7818, e-mail: pesposit@cvm.fda.gov. sent to the contact person listed in the
Grants Management Office Contact:
SUPPLEMENTARY INFORMATION: Natchez FOR FURTHER INFORMATION CONTACT
Delores Dickenson, U.S. Department of
Health and Human Services, Animal Supply Co., 201 John R. Junkin section of this document.
Administration for Children and Dr., Natchez, MS 39120, has requested FOR FURTHER INFORMATION CONTACT: Igor
Families, ACYF—Head Start Bureau, that FDA withdraw approval of NADA Cerny, Center for Drug Evaluation and
330 C Street SW., Switzer Room 2220, 121–557 for THR Worm (dichlorophene Research (HFD–21), Food and Drug
Washington, DC 20447, Phone: 202– and toluene) Capsules used in dogs and Administration, 5600 Fishers Lane,
260–7622, E-mail: cats for removal of certain intestinal Rockville, Maryland 20857, 301–827–
dedickenson@acf.hhs.gov. parasites. This action is requested 7001, e-mail: cerny@cder.fda.gov.
because the product is no longer
VIII. Other Information SUPPLEMENTARY INFORMATION: FDA is
manufactured or marketed.
Therefore, under authority delegated requesting nominations for voting
Applicants will not be sent consumer representatives to all of its
acknowledgements of received to the Commissioner of Food and Drugs
(21 CFR 5.10), redelegated to the Center advisory committees identified in
applications. section I of this document.
Notice: Beginning with FY 2006, the for Veterinary Medicine (21 CFR 5.84),
Administration for Children and and in accordance with 21 CFR 514.115 I. Functions
Families (ACF) will no longer publish Withdrawal of approval of applications,
The functions of advisory committees
grant announcements in the Federal notice is given that approval of NADA
under the purview of CDER are listed in
Register. Beginning October 1, 2005, 121–557 and all supplements and
the following paragraphs.
applicants will be able to find a amendments thereto, is hereby
synopsis of all ACF grant opportunities withdrawn, effective April 25, 2005. A. Arthritis Advisory Committee
and apply electronically for In a final rule published elsewhere in
The committee reviews and evaluates
opportunities via: http:// this issue of the Federal Register, FDA
data concerning the safety and
www.Grants.gov. Applicants will also be is amending the animal drug regulations
effectiveness of marketed and
able to find the complete text of all ACF to reflect the withdrawal of approval of
investigational human drug products for
grant announcements on the ACF Web this NADA.
use in the treatment of arthritis,
site located at: http://www.acf.hhs.gov/ Dated: March 31, 2005. rheumatism, and related diseases and
grants/index.html. Catherine P. Beck, makes appropriate recommendations to
Dated: March 31, 2005. Acting Director, Center for Veterinary the Commissioner of Food and Drugs
Joan E. Ohl, Medicine. (the Commissioner).
Commissioner, Administration on Children, [FR Doc. 05–7338 Filed 4–12–05; 8:45 am]
B. Anti-Infective Drugs Advisory
Youth and Families. BILLING CODE 4160–01–S
Committee
[FR Doc. 05–7030 Filed 4–12–05; 8:45 am]
The committee reviews and evaluates
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND available data concerning the safety and
HUMAN SERVICES effectiveness of marketed and
DEPARTMENT OF HEALTH AND investigational human drug products for
Food and Drug Administration use in the treatment of infectious
HUMAN SERVICES
diseases and disorders and makes
Request for Nominations for Voting appropriate recommendations to the
Food and Drug Administration Consumer Representative Members on Commissioner.
[Docket No. 2005N–0059] Public Advisory Committees
C. Cardiovascular and Renal Drugs
Withdrawal of Approval of a New AGENCY: Food and Drug Administration, Advisory Committee
Animal Drug Application; HHS.
ACTION: Notice. The committee reviews and evaluates
Dichlorophene and Toluene Capsules available data concerning the safety and
AGENCY: Food and Drug Administration, SUMMARY: The Food and Drug effectiveness of marketed and
HHS. Administration (FDA) is requesting investigational human drug products for
ACTION: Notice. nominations for voting consumer use in the treatment of cardiovascular
representatives to serve on its advisory and renal disorders and makes
SUMMARY: The Food and Drug committees that are under the purview appropriate recommendations to the
Administration (FDA) is withdrawing of the Center for Drug Evaluation and Commissioner.
approval of a new animal drug Research (CDER).
application (NADA) for dichlorophene FDA has a special interest in ensuring D. Dermatologic and Ophthalmic Drugs
and toluene capsules used in dogs and that women, minority groups, and Advisory Committee
cats for removal of certain intestinal individuals with disabilities are The committee reviews and evaluates
parasites. In a final rule published adequately represented on its advisory available data concerning the safety and

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