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SUBJECT CATEGORY: New Animal Drugs for Use in Animal Feeds; Semduramicin, Virginiamycin, and Roxarsone
DOCUMENT SUMMARY: The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a new animal drug application (NADA) filed by Phibro Animal Health. The NADA provides for the use of approved, singleingredient Type A medicated articles containing semduramicin, virginiamycin, and roxarsone to formulate threeway combination drug Type C medicated feeds for broiler chickens.
SUMMARY: Semduramicin, virginiamycin, and roxarsone,
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 (HFA305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852, between 9 a.m. and 4 p.m., Monday through Friday.
The agency has determined under 21 CFR 25.33(a)(2) 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. 801808.
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 558NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS
1. The authority citation for 21 CFR part 558 continues to read as follows:
Authority: 21 U.S.C. 360b, 371.
2. Section 558.555 is amended by adding paragraph (d)(8) to read as follows:
Sec. 558.555 Semduramicin.
* * * * *
(d) * * *
(8) Amount. Semduramicin 22.7 grams with virginiamycin 20 grams and roxarsone 22.7 to 45.4 grams/ton.
(i) Indications for use. For the prevention of coccidiosis caused
by Eimeria tenella, E. acervulina, E. maxima, E. brunetti, E. necatrix,
and E. mivati/mitis; for prevention of necrotic enteritis caused by
Clostridium perfringens susceptible to virginiamycin; and for increased
rate of weight gain, improved feed efficiency, and improved pigmentation.
(ii) Limitations. Feed continuously as sole ration throughout
growing period. Withdraw 5 days before slaughter. For broiler chickens
only. Do not feed to laying hens. Use as sole source of organic
arsenic. Poultry should have access to drinking water at all times.
Drug overdose or lack of water may result in leg weakness. Roxarsone
provided by No. 046573; semduramicin and virginiamycin provided by No. 066104 in Sec. 510.600(c) of this chapter.
3. Section 558.635 is amended by revising paragraph (d)(4)(vii) to read as follows:
Sec. 558.635 Virginiamycin.
* * * * *
(d) * * *
(4) * * *
(vii) Semduramicin alone or with roxarsone as in Sec. 558.555.
Dated: March 11, 2004.
Linda Tollefson,
Deputy Director, Center for Veterinary Medicine.
[FR Doc. 046247 Filed 31904; 8:45 am]
BILLING CODE 416001S
FOR FURTHER INFORMATION CONTACT Janis R. Messenheimer, Center for
Veterinary Medicine (HFV135), Food and Drug Administration, 7500
Standish Pl., Rockville, MD 20855, 3018277578, email:
jmessenh@cvm.fda.gov.
14 CFR Part 39 40 CFR Part 52 14 CFR Part 71 33 CFR Part 165 50 CFR Part 679 26 CFR Part 1 40 CFR Part 180 47 CFR Part 73 50 CFR Part 17 33 CFR Part 117 44 CFR Part 67 50 CFR Part 648 14 CFR Part 97 33 CFR Part 100 40 CFR Part 63 26 CFR Part 301 50 CFR Part 622 39 CFR Part 111 40 CFR Part 300 44 CFR Part 65 50 CFR Part 660 40 CFR Part 271 40 CFR Parts 52 and 81 47 CFR Part 64 50 CFR Part 665 49 CFR Part 571 44 CFR Part 64 21 CFR Part 522 14 CFR Part 23 47 CFR Part 76