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Federal Register / Vol. 72, No.

4 / Monday, January 8, 2007 / Rules and Regulations 653

Issued in College Park, Georgia, on Management (HFA–305), Food and Drug greater than 30 grams per ton (360
December 14, 2006. Administration, 5630 Fishers Lane, rm. milligrams per head per day). * * *
Kathy Kutch, 1061, Rockville, MD 20852, between 9 * * * * *
Manager, System Support Group, Eastern a.m. and 4 p.m., Monday through (vii) Amount per ton. Monensin, 10 to
Service Center. Friday. 40 grams.
[FR Doc. 06–9996 Filed 1–5–07; 8:45 am] FDA has carefully considered the * * * * *
BILLING CODE 4910–13–M potential environmental impact of this (b) Limitations. For cattle fed in
action and has concluded that the action confinement for slaughter, feed at a rate
will not have a significant impact on the of 0.14 to 0.42 milligram per pound of
DEPARTMENT OF HEALTH AND human environment and that an body weight per day, depending upon
HUMAN SERVICES environmental impact statement is not the severity of challenge, up to
required. FDA’s finding of no significant maximum of 480 milligrams per head
Food and Drug Administration impact and the evidence supporting that per day.
finding, contained in an environmental
21 CFR Part 558 assessment, may be seen in the Division * * * * *
of Dockets Management (address above) Dated: December 19, 2006.
New Animal Drugs For Use in Animal between 9 a.m. and 4 p.m., Monday Steven D. Vaughn,
Feeds; Monensin through Friday. Director, Office of New Animal Drug
AGENCY: Food and Drug Administration, This rule does not meet the definition Evaluation, Center for Veterinary Medicine.
HHS. of ‘‘rule’’ in 5 U.S.C. 804(3)(A) because [FR Doc. E7–4 Filed 1–5–07; 8:45 am]
ACTION: Final rule. it is a rule of ‘‘particular applicability.’’ BILLING CODE 4160–01–S
Therefore, it is not subject to the
SUMMARY: The Food and Drug congressional review requirements in 5
Administration (FDA) is amending the U.S.C. 801–808. ENVIRONMENTAL PROTECTION
animal drug regulations to reflect AGENCY
List of Subjects in 21 CFR Part 558
approval of a supplemental new animal
drug application (NADA) filed by Animal drugs, Animal feeds. 40 CFR Part 52
Elanco Animal Health. The ■ Therefore, under the Federal Food,
Drug, and Cosmetic Act and under [EPA–R03–OAR–2006–0648; FRL–8266–1]
supplemental NADA revises the
concentration of monensin in Type C authority delegated to the Commissioner Approval and Promulgation of Air
medicated feeds used for improved feed of Food and Drugs and redelegated to Quality Implementation Plans; Virginia;
efficiency, and for the prevention and the Center for Veterinary Medicine, 21 Identification of the Northern Virginia
control of coccidiosis in cattle fed in CFR part 558 is amended as follows: PM2.5 Nonattainment Area
confinement for slaughter.
DATES: This rule is effective January 8, PART 558—NEW ANIMAL DRUGS FOR AGENCY: Environmental Protection
2007. USE IN ANIMAL FEEDS Agency (EPA).
FOR FURTHER INFORMATION CONTACT: Eric ■ 1. The authority citation for 21 CFR ACTION: Direct final rule.
S. Dubbin, Center for Veterinary part 558 continues to read as follows:
Medicine (HFV–126), Food and Drug SUMMARY: EPA is taking direct final
Administration, 7500 Standish Pl., Authority: 21 U.S.C. 360b, 371. action to approve revisions to the
Rockville, MD 20855, 301–827–0232, e- ■ 2. Section 558.355 is amended as Virginia State Implementation Plan
mail: eric.dubbin@fda.hhs.gov. follows: (SIP). The revision consists of the
a. Revise paragraph (d)(2); addition of counties in Northern
SUPPLEMENTARY INFORMATION: Elanco
b. Revise the introductory text of Virginia which were designated as
Animal Health, A Division of Eli Lilly
paragraphs (f)(3)(i) and (f)(3)(vii); nonattainment for the fine particulate
& Co., Lilly Corporate Center,
c. Revise paragraph (f)(3)(vii)(b); (PM2.5) national ambient air quality
Indianapolis, IN 46285, filed a d. Amend paragraph (f)(3)(i)(b)(1) by standard (NAAQS). EPA is approving
supplement to NADA 95–735 that revising the second sentence and adding this revision in accordance with the
provides for use of RUMENSIN 80 a new third sentence. requirements of the Clean Air Act.
(monensin) Type A medicated articles. The revisions read as follows:
The supplement revises the DATES: This rule is effective on March 9,
concentration of monensin in Type C § 558.355 Monensin. 2007 without further notice, unless EPA
medicated feeds used for improved feed receives adverse written comment by
* * * * *
efficiency, and for the prevention and (d) * * * February 7, 2007. If EPA receives such
control of coccidiosis in cattle fed in (2) Type C cattle feeds containing 40 comments, it will publish a timely
confinement for slaughter. The grams or less monensin per ton shall withdrawal of the direct final rule in the
supplemental NADA is approved as of bear an expiration date of 30 days after Federal Register and inform the public
December 1, 2006, and the regulations its date of manufacture. that the rule will not take effect.
in 21 CFR 558.355 are amended to (f) * * * ADDRESSES: Submit your comments,
reflect the approval. The basis of (3) * * * identified by Docket ID Number EPA-
approval is discussed in the freedom of (i) [Amount per ton]. Monensin, 5 to R03-OAR–2006–0648 by one of the
information summary. 40 grams. following methods:
In accordance with the freedom of (b) * * * A. www.regulations.gov. Follow the
information provisions of 21 CFR part (1) Limitations. * * * Feed on-line instructions for submitting
sroberts on PROD1PC70 with RULES

20 and 21 CFR 514.11(e)(2)(ii), a continuously in complete feed at a rate comments.


summary of safety and effectiveness of 50 to 480 milligrams of monensin per B. E-mail: miller.linda@epa.gov.
data and information submitted to head per day. No additional C. Mail: EPA–R03–OAR–2006–0648,
support approval of this application improvement in feed efficiency has been Linda Miller, Acting Chief, Air Quality
may be seen in the Division of Dockets shown from feeding monensin at levels Planning and Analysis Branch,

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