Animal drugs, feeds, and related products: Amprolium,
[Federal Register: September 6, 2006 (Volume 71, Number 172)]
[Rules and Regulations]
[Page 52429-52430]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr06se06-15]
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
New Animal Drugs For Use in Animal Feeds; Amprolium
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule.
SUMMARY: The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a supplemental new animal drug application (NADA) filed by Merial Ltd. The supplemental NADA provides for formulation of Type C medicated calf feeds containing amprolium used for the prevention and treatment of coccidiosis at a broader range of concentrations.
DATES: This rule is effective September 6, 2006.
FOR FURTHER INFORMATION CONTACT: Joan C. Gotthardt, Center for Veterinary Medicine (HFV-130), Food and Drug Administration, 7500 Standish Pl., Rockville, MD 20855, 301-827-7571, e-mail: joan.gotthardt@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: Merial Ltd., 3239 Satellite Blvd., Bldg. 500, Duluth, GA 30096-4640, filed a supplement to NADA 12-350 for CORID (amprolium) Type A Medicated Article 25%. The supplemental NADA provides for formulation of Type C medicated calf feeds used for the prevention and treatment of coccidiosis at a broader range of concentrations. The supplemental NADA is approved as of July 19, 2006, and 21 CFR 558.55 is amended to reflect the approval. The basis of approval is discussed in the freedom of information summary.
In accordance with the freedom of information provisions of 21 CFR part 20 and 21 CFR 514.11(e)(2)(ii), a summary of safety and effectiveness data and information submitted to support approval of this application may be seen in the Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852, between 9 a.m. and 4 p.m., Monday through Friday.
FDA has determined under 21 CFR 25.33(a)(1) that this action is of a type that does not individually or cumulatively have a significant effect on the human environment. Therefore, neither an environmental assessment nor an environmental impact statement is required.
This rule does not meet the definition of ``rule'' in 5 U.S.C. 804(3)(A) because it is a rule of ``particular applicability.'' Therefore, it is not subject to the congressional review requirements in 5 U.S.C. 801-808.
List of Subjects in 21 CFR Part 558
Animal drugs, Animal feeds.
0 Therefore, under the Federal Food, Drug, and Cosmetic Act and under authority delegated to the Commissioner of Food and Drugs and redelegated to the Center for Veterinary Medicine, 21 CFR part 558 is amended as follows:
PART 558--NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS
0 1. The authority citation for 21 CFR part 558 continues to read as follows:
Authority: 21 U.S.C. 360b, 371. 0 2. Revise paragraph (d)(1) of Sec. 558.55 to read as follows:
Sec. 558.55 Amprolium.
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(d) * * *
(1) Cattle. It is used as follows:
[[Page 52430]]
Amprolium in Grams per Ton
Indications for Use
Limitations
Sponsor
(i) 113.5 to 11, 350; to provide 5 Calves: As an aid in the Top-dress on or mix in the daily ration. Feed for 21 days during 050604 milligrams (mg) per kilogram of prevention of coccidiosis periods of exposure or when experience indicates that coccidiosis is body weight per day.
caused by Eimeria bovis and likely to be a hazard; as sole source of amprolium. Withdraw 24 hours E. zurnii before slaughter. A withdrawal period has not been established for this product in preruminating calves. Do not use in calves to be processed for veal
(ii) 113.5 to 11, 350; to provide Calves: As an aid in the Top-dress on or mix in the daily ration. Feed for 5 days; as sole 050604 10 mg per kilogram of body weight treatment of coccidiosis source of amprolium. Withdraw 24 hours before slaughter. A withdrawal per day.
caused by Eimeria bovis and period has not been established for this product in preruminating E. zurnii
calves. Do not use in calves to be processed for veal. For a satisfactory diagnosis, a microscopic examination of the feces should be done by a veterinarian or diagnostic laboratory before treatment; when treating outbreaks, the drug should be administered promptly after diagnosis is determined
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Dated: August 22, 2006. Steven D. Vaughn, Office of New Animal Drug Evaluation, Center for Veterinary Medicine.
[FR Doc. E6-14673 Filed 9-5-06; 8:45 am]
BILLING CODE 4160-01-S
