New Animal Drugs for Use in Animal Feeds; Tiamulin
Federal Register, Volume 77 Issue 78 (Monday, April 23, 2012)
Federal Register Volume 77, Number 78 (Monday, April 23, 2012)
Rules and Regulations
Pages 24138-24139
From the Federal Register Online via the Government Printing Office www.gpo.gov
FR Doc No: 2012-9708
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
Docket No. FDA-2012-N-0002
New Animal Drugs for Use in Animal Feeds; Tiamulin
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule.
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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 Novartis Animal Health US, Inc. The supplemental NADA provides for approval of a new concentration of a Type A medicated article.
DATES: This rule is effective April 23, 2012.
FOR FURTHER INFORMATION CONTACT: Cindy L. Burnsteel, Center for Veterinary Medicine (HFV-130), Food and Drug Administration, 7500 Standish Pl., Rockville, MD 20855, 240-276-8341, email: cindy.burnsteel@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: Novartis Animal Health US, Inc. (Novartis), 3200 Northline Ave., Suite 300, Greensboro, NC 27408, filed a supplement to NADA 139-472 for DENAGARD (tiamulin hydrogen fumarate) Type A medicated articles for use of a new product formulation in medicated swine feed. The supplemental NADA is approved as of January 6, 2012, and the regulations in 21 CFR 558.4 and 558.600 are amended to reflect the approval.
The Agency has determined under 21 CFR 25.33 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.
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
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The authority citation for 21 CFR part 558 continues to read as follows:
Authority: 21 U.S.C. 360b, 371.
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In paragraph (d) of Sec. 558.4, in the ``Category II'' table, revise the entries for ``Tiamulin'' to read as follows:
Sec. 558.4 Requirement of a medicated feed mill license.
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(d) * * *
Category II
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Assay limits Assay limits
Drug percent \1\ Type Type B maximum percent \1\ Type
A (100x) B/C \2\
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Tiamulin hydrogen fumarate............................. 90-115 10 g/lb 90-115/70-130
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\1\ Percent of labeled amount.
\2\ Values given represent ranges for either Type B or Type C medicated feeds. For those drugs that have two
range limit, the first set is for a Type B medicated feed and the second set is for a Type C medicated feed.
These values (ranges) have been assigned in order to provide for the possibility of dilution of a Type B
medicated feed with lower assay limits to make a Type C medicated feed.
Page 24139
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In Sec. 558.600, revise paragraph (a) and the heading of the first column in the table in paragraph (e)(1) to read as follows:
Sec. 558.600 Tiamulin.
(a) Specifications. Type A article containing 363.2 grams of tiamulin hydrogen fumarate per pound.
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(e) * * *
(1) * * *
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Tiamulin hydrogen fumarate in
grams per ton * * * * * * * * * * * *
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Dated: April 17, 2012.
Steven D. Vaughn,
Director, Office of New Animal Drug Evaluation, Center for Veterinary Medicine.
FR Doc. 2012-9708 Filed 4-20-12; 8:45 am
BILLING CODE 4160-01-P
