96-30589. Ophthalmic and Topical Dosage Form New Animal Drugs; Change of Sponsor  

  • [Federal Register Volume 61, Number 232 (Monday, December 2, 1996)]
    [Rules and Regulations]
    [Page 63712]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 96-30589]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    21 CFR Part 524
    
    
    Ophthalmic and Topical Dosage Form New Animal Drugs; Change of 
    Sponsor
    
    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 the change of sponsor for an approved new 
    animal drug application (NADA) for Biocraft Laboratories, Inc., and A. 
    H. Robins Co.
    
    EFFECTIVE DATE: December 2, 1996.
    
    FOR FURTHER INFORMATION CONTACT: Thomas J. McKay, Center for Veterinary 
    Medicine (HFV-102), Food and Drug Administration, 7500 Standish Pl., 
    Rockville, MD 20855, 301-827-0213.
    
    SUPPLEMENTARY INFORMATION: A. H. Robins Co., P.O. Box 518, Fort Dodge, 
    IA 50501-0518, and Biocraft Laboratories, Inc., 92 Route 46, Elmwood 
    Park, NJ 07407, are no longer cosponsors of NADA 140-889. This 
    arrangement was terminated sometime ago, but the agency failed to 
    reflect the change in the regulations. Biocraft Laboratories, Inc., now 
    exclusively owns NADA 140-889 and A. H. Robins Co. is the sponsor of 
    new NADA 141-003. A. H. Robins Co. filed a supplement to NADA 140-889 
    to provide for the establishment of a new NADA. Therefore, the agency 
    is amending 21 CFR 524.1600a to reflect the change of sponsorship.
    
    List of Subjects in 21 CFR Part 524
    
        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 524 is 
    amended as follows:
    
    PART 524--OPHTHALMIC AND TOPICAL DOSAGE FORM NEW ANIMAL DRUGS
    
        1. The authority citation for 21 CFR part 524 continues to read as 
    follows:
    
        Authority: Sec. 512 of the Federal Food, Drug, and Cosmetic Act 
    (21 U.S.C. 360b).
    
    
    Sec. 524.1600a  [Amended]
    
        2. Section 524.1600a Nystatin, neomycin, thiostrepton, and 
    triamcinolone acetonide ointment is amended in paragraph (b) by 
    removing ``See Nos. 000031/000332 (cosponsors), 000069, 025463, 051259, 
    and 053501 in Sec. 510.600(c) of this chapter'' and by adding in its 
    place ``See Nos. 000031, 000069, 000332, 025463, 051259, and 053501 in 
    Sec. 510.600(c) of this chapter''.
    
        Dated: November 21, 1996.
    Robert C. Livingston,
    Director, Office of New Animal Drug Evaluation, Center for Veterinary 
    Medicine.
    [FR Doc. 96-30589 Filed 11-29-96; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Effective Date:
12/2/1996
Published:
12/02/1996
Department:
Health and Human Services Department
Entry Type:
Rule
Action:
Final rule.
Document Number:
96-30589
Dates:
December 2, 1996.
Pages:
63712-63712 (1 pages)
PDF File:
96-30589.pdf
CFR: (2)
21 CFR 510.600(c)
21 CFR 524.1600a