96-123. New Animal Drugs and Related Products; Change of Sponsor  

  • [Federal Register Volume 61, Number 3 (Thursday, January 4, 1996)]
    [Rules and Regulations]
    [Page 260]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 96-123]
    
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    21 CFR Part 522
    
    
    New Animal Drugs and Related Products; 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 a change of sponsor for a new animal drug 
    application (NADA) from Fort Dodge Laboratories to Wildlife 
    Laboratories, Inc.
    
    EFFECTIVE DATE: January 4, 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: Fort Dodge Laboratories, Fort Dodge, IA 
    50501, has informed FDA that it has transferred ownership of, and all 
    rights and interests in approved NADA 47-870 (Etorphine hydrochloride 
    injection) to Wildlife Laboratories, Inc., 1401 Duff Dr., suite 600, 
    Fort Collins, CO 80524. This NADA was originally owned by American 
    Cyanamid Co. and transferred to Fort Dodge Laboratories but was 
    inadvertently not codified in the regulations. Accordingly, FDA is 
    amending the regulations in 21 CFR 522.883 to reflect the change of 
    sponsor.
    
    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).
    
    Sec. 522.883  [Amended]
    
         2. Section 522.883 Etorphine hydrochloride injection is amended in 
    paragraph (c) by removing ``010042'' and adding in its place 
    ``053923''.
    
        Dated: December 22, 1995.
    Robert C. Livingston,
    Director, Office of New Animal Drug Evaluation, Center for Veterinary 
    Medicine.
    [FR Doc. 96-123 Filed 1-3-96; 8:45 am]
    BILLING CODE 4160-01-F
    
    

Document Information

Effective Date:
1/4/1996
Published:
01/04/1996
Department:
Health and Human Services Department
Entry Type:
Rule
Action:
Final rule.
Document Number:
96-123
Dates:
January 4, 1996.
Pages:
260-260 (1 pages)
PDF File:
96-123.pdf
CFR: (1)
21 CFR 522.883