[Federal Register Volume 72, Number 166 (Tuesday, August 28, 2007)]
[Notices]
[Page 49282]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: E7-16985]



[[Page 49282]]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 2007N-0324]


Withdrawal of Approval of a New Animal Drug Application; 
Bacitracin Zinc

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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SUMMARY: The Food and Drug Administration (FDA) is withdrawing approval 
of a new animal drug application (NADA) for a bacitracin zinc Type A 
medicated article. In a final rule published elsewhere in this issue of 
the Federal Register, FDA is amending the animal drug regulations to 
remove portions reflecting approval of this NADA.

FOR FURTHER INFORMATION CONTACT: Pamela K. Esposito, Center for 
Veterinary Medicine (HFV-212), Food and Drug Administration, 7519 
Standish Pl., Rockville, MD 20855, 301-827-7818; e-mail: 
[email protected].

SUPPLEMENTARY INFORMATION: Pennfield Oil Co., 14040 Industrial Rd., 
Omaha, NE 68144, has requested that FDA withdraw approval of NADA 128-
550 for ANCHOR Zinc Bacitracin Type A medicated article because the 
product is not manufactured or marketed.
    Therefore, under authority delegated to the Commissioner of Food 
and Drugs and redelegated to the Center for Veterinary Medicine, and in 
accordance with Sec.  514.115 Withdrawal of approval of applications 
(21 CFR 514.115), notice is given that approval of NADA 128-550, and 
all supplements and amendments thereto, are hereby withdrawn, effective 
August 28, 2007.
    In a final rule published elsewhere in this issue of the Federal 
Register, FDA is amending the animal drug regulations to reflect the 
withdrawal of approval of this NADA.

    Dated: August 20, 2007.
Stephen F. Sundlof,
Director, Center for Veterinary Medicine.
[FR Doc. E7-16985 Filed 8-27-07; 8:45 am]
BILLING CODE 4160-01-S