[Federal Register Volume 73, Number 225 (Thursday, November 20, 2008)]
[Rules and Regulations]
[Page 70276]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: E8-27646]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 520

[Docket No. FDA-2008-N-0039]


Oral Dosage Form New Animal Drugs; Amprolium; Correction

AGENCY: Food and Drug Administration, HHS.

ACTION: Correcting amendments.

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SUMMARY: The Food and Drug Administration (FDA) is correcting a 
document amending the animal drug regulations to reflect approval of a 
supplemental new animal drug application (NADA) that appeared in the 
Federal Register of August 6, 2008 (73 FR 45610). FDA is correcting a 
paragraph designating the sponsors of approved applications for oral 
dosage forms of amprolium. This correction is being made to improve the 
accuracy of the animal drug regulations.

DATES: This rule is effective November 20, 2008.

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: 
[email protected].

SUPPLEMENTARY INFORMATION: For reasons set forth in this preamble, FDA 
is correcting 21 CFR part 520 as follows:

List of Subjects in 21 CFR Part 520

    Animal drugs.

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Therefore, under the Federal Food, Drug, and Cosmetic Act and under the 
authority delegated to the Commissioner of Food and Drugs and 
redelegated to the Center for Veterinary Medicine, 21 CFR part 520 is 
corrected by making the following amendment:

PART 520--ORAL DOSAGE FORM NEW ANIMAL DRUGS

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1. The authority citation for 21 CFR part 520 continues to read as 
follows:

    Authority: 21 U.S.C. 360b.


Sec.  520.100  [Corrected]

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2. In Sec.  520.100(b)(2), remove ``Nos. 051311 and 066104'' and add in 
its place ``No. 66104''.

    Dated: October 17, 2008.
Bernadette Dunham,
Director, Center for Veterinary Medicine.
[FR Doc. E8-27646 Filed 11-19-08; 8:45 am]
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