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SUBJECT CATEGORY: New Animal Drugs for Use in Animal Feeds; Carbadox and Oxytetracycline
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 carbadox and oxytetracycline to formulate twoway combination drug Type C medicated feeds for swine.
SUMMARY: Carbadox and oxytetracycline,
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 558.115 is amended by adding paragraph (d)(4) to read as follows:
Sec. 558.115 Carbadox.
* * * * *
(d) * * *
(4) Amount. Carbadox, 10 to 25 grams per ton of feed; plus oxytetracycline, 10 milligrams per pound of body weight.
(i) Indications for use. For treatment of bacterial enteritis
caused by Escherichia coli and S. choleraesuis susceptible to
oxytetracycline, for treatment of bacterial pneumonia caused by
Pasteurella multocida susceptible to oxytetracycline; and for increased rate of weight gain and improved feed efficiency.
(ii) Limitations. Feed continuously for 7 to 14 days. Not for use
in pregnant swine or swine intended for breeding purposes. Do not feed to swine within 42 days of slaughter.
3. Section 558.450 is amended by redesignating paragraph (d)(3)(i) as
paragraph (d)(3)(iv); and by adding new paragraph (d)(3)(i) to read as follows:
Sec. 558.450 Oxytetracycline.
* * * * *
(d) * * *
(3) * * *
(i) Carbadox as in Sec. 558.115 of this chapter.
* * * * *
Dated: August 2, 2004.
Linda Tollefson,
Acting Director, Center for Veterinary Medicine.
[FR Doc. 0418844 Filed 81704; 8:45 am]
BILLING CODE 416001S
FOR FURTHER INFORMATION CONTACT Joan C. Gotthardt, Center for
Veterinary Medicine (HFV130), Food and Drug Administration, 7500 Standish Pl., Rockville, MD 20855, 3018277571, email:
joan.gotthardt@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 50 CFR Part 622 26 CFR Part 301 39 CFR Part 111 40 CFR Part 300 50 CFR Part 660 44 CFR Part 65 40 CFR Parts 52 and 81 40 CFR Part 271 47 CFR Part 64 50 CFR Part 665 47 CFR Part 76 50 CFR Part 229 14 CFR Part 23 14 CFR Part 25 21 CFR Part 522