98-4081. Animal Drugs, Feeds, and Related Products; Cephapirin Sodium for Intramammary Infusion; Redesignation  

  • [Federal Register Volume 63, Number 33 (Thursday, February 19, 1998)]
    [Rules and Regulations]
    [Page 8349]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 98-4081]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    
    21 CFR Parts 526 and 529
    
    
    Animal Drugs, Feeds, and Related Products; Cephapirin Sodium for 
    Intramammary Infusion; Redesignation
    
    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 redesignate a section of those regulations. A 
    section reflecting approval of an intramammary product is redesignated 
    from certain other dosage form new animal drugs to intramammary dosage 
    forms to reflect the correct designation of the product.
    
    EFFECTIVE DATE: February 19, 1998.
    FOR FURTHER INFORMATION CONTACT: David L. Gordon, Center for Veterinary 
    Medicine (HFV-6), Food and Drug Administration, 7500 Standish Pl., 
    Rockville, MD 20855, 301-594-1739.
    
    SUPPLEMENTARY INFORMATION: The animal drug regulations in part 529 (21 
    CFR part 529) provide for codification of certain other dosage form new 
    animal drugs. The regulations in part 526 (21 CFR part 526) provide for 
    codification of intramammary dosage forms. Cephapirin sodium for 
    intramammary infusion was inadvertently codified as Sec. 529.365. At 
    this time, the animal drug regulations are amended to redesignate 
    Sec. 529.365 as Sec. 526.365.
    
    List of Subjects
    
    21 CFR Parts 526 and 529
    
        Animal drugs.
        Therefore, under the Federal Food, Drug, and Cosmetic Act and under 
    the authority delegated to the Commissioner of Food and Drugs and 
    redelegated to the Center for Veterinary Medicine, 21 CFR parts 526 and 
    529 are amended as follows:
    
    PART 526--INTRAMAMMARY DOSAGE FORMS
    
    PART 529--CERTAIN OTHER DOSAGE FORM NEW ANIMAL DRUGS
    
        1. The authority citations for 21 CFR parts 526 and 529 continue to 
    read as follows:
    
        Authority: 21 U.S.C. 360b.
    
    
    Sec. 529.365  [Redesignated as Sec. 526.365]
    
        2. Section 529.365 is redesignated as Sec. 526.365.
    
        Dated: February 5, 1998.
    Andrew J. Beaulieau,
    Deputy Director, Office of New Animal Drug Evaluation, Center for 
    Veterinary Medicine.
    [FR Doc. 98-4081 Filed 2-18-98; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Effective Date:
2/19/1998
Published:
02/19/1998
Department:
Food and Drug Administration
Entry Type:
Rule
Action:
Final rule.
Document Number:
98-4081
Dates:
February 19, 1998.
Pages:
8349-8349 (1 pages)
PDF File:
98-4081.pdf
CFR: (1)
21 CFR 529.365