94-12289. New Animal Drugs for Use in Animal Feeds; Salinomycin in Combination With Bacitracin Zinc, or Lincomycin, or Roxarsone  

  • [Federal Register Volume 59, Number 97 (Friday, May 20, 1994)]
    [Unknown Section]
    [Page 0]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 94-12289]
    
    
    [[Page Unknown]]
    
    [Federal Register: May 20, 1994]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    21 CFR Part 558
    
     
    
    New Animal Drugs for Use in Animal Feeds; Salinomycin in 
    Combination With Bacitracin Zinc, or Lincomycin, or Roxarsone
    
    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 three abbreviated new animal 
    drug applications (ANADA's) filed by Hoechst-Roussel Agri-Vet Co. The 
    ANADA's provide for using approved Type A medicated articles to make 
    Type C medicated broiler feeds containing salinomycin with bacitracin 
    zinc, salinomycin with lincomycin, or salinomycin with roxarsone.
    
    EFFECTIVE DATE: May 20, 1994.
    
    FOR FURTHER INFORMATION CONTACT: Charles J. Andres, Center For 
    Veterinary Medicine (HFV-128), Food and Drug Administration, 7500 
    Standish Pl., Rockville, MD 20855, 301-594-1602.
    
    SUPPLEMENTARY INFORMATION: Hoechst-Roussel Agri-Vet Co., P.O. Box 2500, 
    Somerville, NJ 08876-1258, filed the following ANADA's:
        ANADA 200-089, salinomycin with bacitracin zinc, which provides for 
    using approved single ingredient Type A medicated articles to make Type 
    C medicated broiler feeds containing 40 to 60 grams per ton (g/t) 
    salinomycin sodium activity and 10 to 50 g/t bacitracin zinc for 
    prevention of coccidiosis and for increased rate of weight gain. The 
    ANADA is approved as a generic copy of American Cyanamid's new animal 
    drug application (NADA) 139-235.
        ANADA 200-093, salinomycin with lincomycin, which provides for 
    using approved single ingredient Type A medicated articles to make Type 
    C medicated broiler feeds containing 40 to 60 g/t salinomycin sodium 
    activity with 2 to 4 g/t lincomycin, for prevention of coccidiosis and 
    for improved feed efficiency. The ANADA is approved as a generic copy 
    of Agri-Bio Corp.'s NADA 137-537.
        ANADA 200-097, salinomycin with roxarsone, which provides for using 
    approved single ingredient Type A medicated articles to make Type C 
    medicated broiler feeds containing 40 to 60 g/t salinomycin sodium 
    activity with 22.7 to 45.4 g/t roxarsone for prevention of coccidiosis 
    and for improved feed efficiency. The ANADA is approved as a generic 
    copy of Agri-Bio Corp.'s NADA 132-447.
        ANADA's 200-089 and 200-093 are approved as of April 6, 1994. ANADA 
    200-097 is approved as of May 20, 1994. The regulations are amended in 
    21 CFR 558.550 to reflect the approvals.
        These approvals are for use of Type A medicated articles to make 
    Type C medicated feeds. Salinomycin, bacitracin zinc, and lincomycin 
    are Category I drugs which, as provided in Sec. 558.4 (21 CFR 558.4), 
    do not require an approved Form FDA 1900. However, roxarsone is a 
    Category II drug which, as provided in Sec. 558.4, requires an approved 
    Form FDA 1900 for making a Type C medicated feed. Use of salinomycin 
    and roxarsone to make Type C medicated feeds as in ANADA 200-097 
    requires an approved Form FDA 1900.
        In accordance with the freedom of information provisions of part 20 
    (21 CFR part 20) and Sec. 514.11(e)(2)(ii) (21 CFR 514.11(e)(2)(ii)), a 
    summary of safety and effectiveness data and information submitted to 
    support approval of these applications may be seen in the Dockets 
    Management Branch (HFA-305), Food and Drug Administration, rm. 1-23, 
    12420 Parklawn Dr., Rockville, MD 20857, between 9 a.m. and 4 p.m., 
    Monday through Friday.
        The agency has determined under 21 CFR 25.24(d)(1)(ii) that these 
    actions are of a type that do not individually or cumulatively have a 
    significant impact on the human environment. Therefore, neither an 
    environmental assessment nor an environmental impact statement is 
    required.
    
    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
    
        1. The authority citation for 21 CFR part 558 continues to read as 
    follows:
    
        Authority: Secs. 512, 701 of the Federal Food, Drug, and 
    Cosmetic Act (21 U.S.C. 360b, 371).
    
    
    Sec. 558.550  [Amended]
    
        2. Section 558.550 Salinomycin is amended in paragraph (a)(2) by 
    removing ``(b)(1)(vi), (b)(1)(viii), (b)(1)(x), (b)(1)(xi),'' and 
    ``(b)(1)(xii),'' and adding in its place ``(b)(1)(v), (b)(1)(vi), 
    (b)(1)(vii), (b)(1)(viii), (b)(1)(x), (b)(1)(xi), (b)(1)(xii), 
    (b)(1)(xiii),''.
    
        Dated: May 3, 1994.
    Richard H. Teske,
    Acting Director, Center for Veterinary Medicine.
    [FR Doc. 94-12289 Filed 5-19-94; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
05/20/1994
Department:
Health and Human Services Department
Entry Type:
Uncategorized Document
Action:
Final rule.
Document Number:
94-12289
Dates:
May 20, 1994.
Pages:
0-0 (1 pages)
Docket Numbers:
Federal Register: May 20, 1994
CFR: (1)
21 CFR 558.550