95-23250. Implantation or Injectable Dosage Form New Animal Drugs; Oxytetracycline Hydrochloride Injection  

  • [Federal Register Volume 60, Number 182 (Wednesday, September 20, 1995)]
    [Rules and Regulations]
    [Pages 48650-48651]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 95-23250]
    
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    21 CFR Part 522
    
    
    Implantation or Injectable Dosage Form New Animal Drugs; 
    Oxytetracycline Hydrochloride Injection
    
    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 an abbreviated new animal drug 
    application (ANADA) filed by Phoenix Pharmaceutical, Inc. The ANADA 
    provides for intravenous use of oxytetracycline hydrochloride injection 
    in cattle for treatment of certain diseases caused by pathogens 
    sensitive to oxytetracycline.
    EFFECTIVE DATE: September 20, 1995.
    FOR FURTHER INFORMATION CONTACT: Melanie R. Berson, Center For 
    Veterinary Medicine (HFV-135), Food and Drug Administration, 7500 
    Standish Pl., Rockville, MD 20855, 301-594-1643.
    
    SUPPLEMENTARY INFORMATION: Phoenix Pharmaceutical, Inc., 4621 Easton 
    Rd., P.O. Box 6457 Farleigh Station, St. Joseph, MO 64506-0457, filed 
    ANADA 200-068, which provides for intravenous use of oxytetracycline 
    hydrochloride injection in cattle for the treatment of bacterial 
    pneumonia and shipping fever complex associated with Pasteurella spp., 
    bacterial enteritis (scours) caused by Escherichia coli, necrotic 
    pododermatitis (foot rot) and calf diphtheria caused by Spherophorus 
    necrophorus, wooden tongue caused by Actinobacillu lignieresii, wound 
    infection and traumatic injury caused by oxytetracycline susceptible 
    strains of streptococcal and staphylococcal bacteria.
        Phoenix Pharmaceutical, Inc.'s, ANADA 200-068 for oxytetracycline 
    hydrochloride injection is approved as a generic copy of Fermenta's 
    NADA 108-963 for Medamycin-100. The ANADA is approved as of 
    July 31, 1995, and the regulations are amended in 21 CFR 522.1662a(h) 
    to reflect the approval. The basis of approval is discussed in the 
    freedom of information summary.
        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 
    
    [[Page 48651]]
    safety and effectiveness data and information submitted to support 
    approval of this application 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 carefully considered the potential environmental 
    effects of this action. FDA has concluded that the action will not have 
    a significant impact on the human environment, and that an 
    environmental impact statement is not required. The agency's finding of 
    no significant impact and the evidence supporting that finding, 
    contained in an environmental assessment, may be seen in the Dockets 
    Management Branch (address above) between 9 a.m. and 4 p.m., Monday 
    through Friday.
    
    List of Subjects in 21 CFR Part 522
    
        Animal drugs.
        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 522 is 
    amended as follows:
    
    PART 522--IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL DRUGS
    
        1. The authority citation for 21 CFR part 522 continues to read as 
    follows:
    
        Authority: Sec. 512 of the Federal Food, Drug, and Cosmetic Act 
    (21 U.S.C. 360b).
    
        2. Section 522.1662a is amended by revising paragraph (h)(2) to 
    read as follows:
    
    
    Sec. 522.1662a  Oxytetracycline hydrochloride injection.
    
    * * * * *
        (h) * * *
        (2) Sponsors. See 054273 in Sec. 510.600(c) of this chapter for use 
    of 50 and 100 milligrams/milliliter solution, and see No. 057319 in 
    Sec. 510.600(c) for use of 100 milligrams/milliliter solution.
    * * * * *
    
        Dated: September 1, 1995.
    Stephen F. Sundlof,
    Director, Center for Veterinary Medicine.
    [FR Doc. 95-23250 Filed 9-19-95; 8:45 am]
    BILLING CODE 4160-01-F
    
    

Document Information

Effective Date:
9/20/1995
Published:
09/20/1995
Department:
Health and Human Services Department
Entry Type:
Rule
Action:
Final rule.
Document Number:
95-23250
Dates:
September 20, 1995.
Pages:
48650-48651 (2 pages)
PDF File:
95-23250.pdf
CFR: (2)
21 CFR 510.600(c)
21 CFR 522.1662a