94-10458. Oral Dosage Form New Animal Drugs; Change of Sponsor  

  • [Federal Register Volume 59, Number 84 (Tuesday, May 3, 1994)]
    [Unknown Section]
    [Page 0]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 94-10458]
    
    
    [[Page Unknown]]
    
    [Federal Register: May 3, 1994]
    
    
    =======================================================================
    -----------------------------------------------------------------------
    
    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    
    21 CFR Part 520
    
     
    
    Oral Dosage Form New Animal Drugs; Change of Sponsor
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Final rule.
    
    -----------------------------------------------------------------------
    
    SUMMARY: The Food and Drug Administration (FDA) is amending the animal 
    drug regulations to reflect a change of sponsor for three new animal 
    drug applications (NADA's) from SmithKline Beecham Animal Health to 
    Solvay Animal Health, Inc.
    
    EFFECTIVE DATE: May 3, 1994.
    
    FOR FURTHER INFORMATION CONTACT: Benjamin A. Puyot, Center for 
    Veterinary Medicine (HFV-130), Food and Drug Administration, 7500 
    Standish Pl., Rockville, MD 20855, 301-594-1646.
    
    SUPPLEMENTARY INFORMATION: SmithKline Beecham Animal Health, 1600 Paoli 
    Pike, West Chester, PA 19380, has informed FDA that it has transferred 
    ownership of, and all rights and interests in, approved NADA's 49-892, 
    126-232, and 140-909 to Solvay Animal Health, Inc., 1201 Northland Dr., 
    Mendota Heights, MN 55120. Accordingly, FDA is amending the regulations 
    in 21 CFR 520.2260a, 520.2260b, and 520.2260c to reflect the change of 
    sponsor.
    
    List of Subjects in 21 CFR Part 520
    
         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 520 is 
    amended as follows:
    
    PART 520--ORAL DOSAGE FORM NEW ANIMAL DRUGS
    
         1. The authority citation for 21 CFR part 520 continues to read as 
    follows:
    
        Authority: Sec. 512 of the Federal Food, Drug, and Cosmetic Act 
    (21 U.S.C. 360b).
    
    Sec. 520.2260a  [Amended]
    
         2. Section 520.2260a Sulfamethazine oblets and boluses is amended 
    in paragraph (b)(1) by removing ``053571'' and adding in its place 
    ``053501''.
    
    
    Sec. 520.2260b  [Amended]
    
         3. Section 520.2260b Sulfamethazine sustained-release boluses is 
    amended in paragraph (b)(1) by removing ``053571'' and adding in its 
    place ``053501''.
    
    
    Sec. 520.2260c  [Amended]
    
         4. Section 520.2260c Sulfamethazine sustained-release tablets is 
    amended in paragraph (a) by removing ``053571'' and adding in its place 
    ``053501''.
    
        Dated: April 22, 1994.
     Robert C. Livingston,
     Director, Office of New Animal Drug Evaluation, Center for Veterinary 
    Medicine.
    [FR Doc. 94-10458 Filed 5-2-94; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
05/03/1994
Department:
Food and Drug Administration
Entry Type:
Uncategorized Document
Action:
Final rule.
Document Number:
94-10458
Dates:
May 3, 1994.
Pages:
0-0 (1 pages)
Docket Numbers:
Federal Register: May 3, 1994
CFR: (3)
21 CFR 520.2260a
21 CFR 520.2260b
21 CFR 520.2260c