98-25913. New Animal Drugs For Use In Animal Feeds; Narasin and Bacitracin Methylene Disalicylate with Roxarsone  

  • [Federal Register Volume 63, Number 188 (Tuesday, September 29, 1998)]
    [Rules and Regulations]
    [Pages 51823-51824]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 98-25913]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    
    21 CFR Part 558
    
    
    New Animal Drugs For Use In Animal Feeds; Narasin and Bacitracin 
    Methylene Disalicylate with 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 a supplemental new animal drug 
    application (NADA) filed by Alpharma Inc. The supplemental NADA 
    provides for using approved narasin, bacitracin methylene disalicylate 
    (BMD), and roxarsone Type A medicated articles to make Type C medicated 
    broiler chicken feeds.
    
    EFFECTIVE DATE: September 29, 1998
    
    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: Alpharma Inc., One Executive Dr., P.O. Box 
    1399, Fort Lee, NJ 07024, is sponsor of supplemental NADA 140-852 which 
    provides for combining approved Monteban (45 grams per pound 
    (g/lb) narasin), BMD (10, 25, 30, 40, 50, 60, or 75 g/lb 
    bacitracin methylene disalicylate), and 3-Nitro (45.4, 90, or 
    227 g/lb roxarsone) Type A medicated articles to make Type C medicated 
    broiler chicken feeds. The Type C medicated broiler chicken feed 
    containing 54 to 72 g/t narasin, 50 g/t bacitracin methylene 
    disalicylate, and 22.7 to 45.4 g/t roxarsone is used for prevention of 
    coccidiosis caused by Eimeria necatrix, E. tenella, E. acervulina, E. 
    brunetti, E. mivati, and E. maxima, as an aid in the prevention of 
    necrotic enteritis caused or complicated by Clostridium spp. or other 
    organisms susceptible to bacitracin, and for increased rate of weight 
    gain, improved feed efficiency, and improved pigmentation. The Type C 
    medicated broiler chicken feed containing 54 to 72 g/t narasin, 100 to 
    200 g/t bacitracin methylene disalicylate, and 22.7 to 45.4 g/t 
    roxarsone is used for prevention of coccidiosis caused by Eimeria 
    necatrix, E. tenella, E. acervulina, E. brunetti, E. mivati, and E. 
    maxima, as an aid in the control of necrotic enteritis caused or 
    complicated by Clostridium spp. or other organisms susceptible to 
    bacitracin, and for increased rate of weight gain, improved feed 
    efficiency, and improved pigmentation.
        The supplemental NADA is approved as of July 29, 1998, and the 
    regulations are amended by adding 21 CFR 558.363(a)(6), (d)(1)(viii), 
    and (d)(1)(ix) to reflect the approval. The basis for approval is 
    discussed in the freedom of information summary.
        This approval is for use of single ingredient Type A medicated 
    articles to make combination drug Type C medicated feeds. One 
    ingredient, roxarsone, is a Category II drug as defined in 21 CFR 
    558.3(b)(1)(ii). As provided in 21 CFR 558.4(b), an approved form FDA 
    1900 is required to make Type C medicated feed from a Category II drug. 
    Under section 512(m) of the act (21 U.S.C. 360b(m)), as amended by the 
    Animal Drug Availability Act of 1996 (Pub. L. 104-250), medicated feed 
    applications have been replaced by a requirement for feed mill 
    licenses. Therefore, use of Type A medicated articles to make Type C 
    medicated feeds as provided in supplemental NADA 140-852 is limited to 
    manufacture in a licensed feed mill.
        In accordance with the freedom of information provisions of 21 CFR 
    part 20 and 514.11(e)(2)(ii), a summary of safety and effectiveness 
    data and information submitted to support approval of this supplemental 
    application may be seen in the Dockets Management Branch (HFA-305), 
    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) 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.
    
    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: 21 U.S.C. 360b, 371.
        2. Section 558.363 is amended by adding paragraphs (a)(6), 
    (d)(1)(viii), and (d)(1)(ix) to read as follows:
    
    
    Sec. 558.363   Narasin.
    
        (a) * * *
        (6) To 046573: 45 grams per pound with 10, 25, 30, 40, 50, 60, or 
    75 grams per pound bacitracin methylene disalicylate and 45.4, 90, or 
    227 grams per pound roxarsone, paragraphs (d)(1)(viii) and (d)(1)(ix) 
    of this section.
    * * * * *
        (d) * * *
        (1) * * *
        (viii) Amount per ton. Narasin, 54 to 72 grams, and bacitracin 
    methylene disalicylate, 50 grams, with roxarsone, 22.7 to 45.4 grams.
        (A) Indications for use. For prevention of coccidiosis caused by 
    Eimeria necatrix, E. tenella, E. acervulina, E. brunetti, E. mivati, 
    and E. maxima, as an aid in the prevention of necrotic enteritis caused 
    or complicated by Clostridium spp. or other organisms susceptible to 
    bacitracin, and for increased rate of weight gain, improved feed 
    efficiency, and improved pigmentation.
        (B) Limitations. For broiler chickens only. Feed continuously as 
    sole ration. Withdraw 5 days before slaughter. Do not feed to laying 
    hens. Do not allow adult turkeys, horses, or other equines access to 
    narasin formulations. Ingestion of narasin by these species has been 
    fatal. Use as sole source of organic arsenic. Poultry should have 
    access to drinking water at all times. Drug overdose or lack of water 
    intake may result in leg weakness or paralysis. Narasin as provided by 
    000986, bacitracin methylene disalicylate and roxarsone by 046573 in 
    Sec. 510.600(c) of this chapter.
        (ix) Amount per ton. Narasin, 54 to 72 grams, and bacitracin 
    methylene disalicylate, 100 to 200 grams, with roxarsone, 22.7 to 45.4 
    grams.
        (A) Indications for use. For prevention of coccidiosis caused by 
    Eimeria necatrix, E. tenella, E. acervulina, E. brunetti, E. mivati, 
    and E. maxima, as an aid in the control of necrotic enteritis caused or 
    complicated by Clostridium spp. or other organisms susceptible to 
    bacitracin, and for increased rate of weight gain, improved feed 
    efficiency, and improved pigmentation.
        (B) Limitations. For broiler chickens only. Feed continuously as 
    sole ration. Withdraw 5 days before slaughter. Do
    
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    not feed to laying hens. Do not allow adult turkeys, horses, or other 
    equines access to narasin formulations. Ingestion of narasin by these 
    species has been fatal. Use as sole source of organic arsenic. Poultry 
    should have access to drinking water at all times. Drug overdose or 
    lack of water intake may result in leg weakness or paralysis. Narasin 
    as provided by 000986, bacitracin methylene disalicylate and roxarsone 
    by 046573 in Sec. 510.600(c) of this chapter.
    
        Dated: August 27, 1998.
    Stephen F. Sundlof,
    Director, Center for Veterinary Medicine.
    [FR Doc. 98-25913 Filed 9-28-98; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Effective Date:
9/29/1998
Published:
09/29/1998
Department:
Food and Drug Administration
Entry Type:
Rule
Action:
Final rule.
Document Number:
98-25913
Dates:
September 29, 1998
Pages:
51823-51824 (2 pages)
PDF File:
98-25913.pdf
CFR: (2)
21 CFR 510.600(c)
21 CFR 558.363