99-24596. New Animal Drugs; Labeling of Drugs for Use in Milk-Producing Animals; Technical Amendment  

  • [Federal Register Volume 64, Number 183 (Wednesday, September 22, 1999)]
    [Rules and Regulations]
    [Page 51241]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 99-24596]
    
    
    
    [[Page 51241]]
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    
    21 CFR Part 510
    
    
    New Animal Drugs; Labeling of Drugs for Use in Milk-Producing 
    Animals; Technical Amendment
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION:  Final rule; technical amendment.
    
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    SUMMARY: The Food and Drug Administration (FDA) is amending the animal 
    drug regulations concerning labeling of drugs for use in milk-producing 
    animals. This document corrects two outdated cross-references. As 
    amended, the references conform to the current statute and regulations.
    
    EFFECTIVE DATE:  September 22, 1999.
    FOR FURTHER INFORMATION CONTACT: Carol J. Haley, Center for Veterinary 
    Medicine (HFV-6), Food and Drug Administration, 7500 Standish Pl., 
    Rockville, MD 20855, 301-594-1682.
    
    SUPPLEMENTARY INFORMATION: FDA is amending the animal drug regulations 
    in 21 CFR 510.105(a) and (b) concerning labeling of drugs for use in 
    milk-producing animal. Paragraph (a) cites ``Part 540 of this chapter'' 
    and paragraph (b) cites ``section 402(a)(2)(D) of the act''. Because of 
    revisions of the act and the regulations, these cites should be changed 
    to ``Part 526 of this chapter'' and ``section 402(a)(2)(c)(ii) of the 
    act'', respectively. This document amends the regulation accordingly.
        This rule does not meet the definition of ``rule'' in 5 U.S.C. 
    804(3)(A) because it is a rule of ``particular applicability.'' 
    Therefore, it is not subject to the congressional review requirements 
    in 5 U.S.C. 801-808.
    
    List of Subjects in 21 CFR Part 510
    
        Administrative practice and procedure, Animal drugs, Labeling, 
    Reporting and recordkeeping requirements.
        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 part 510 is 
    amended as follows:
    
    PART 510--NEW ANIMAL DRUGS
    
        1. The authority citation for 21 CFR part 510 continues to read as 
    follows:
    
         Authority: 21 U.S.C. 321, 331, 351, 352, 353, 360b, 371, 379e.
    
    Sec. 510.105  [Amended]
    
        2. Section 510.105 Labeling of drugs for use in milk-producing 
    animals is amended in paragraph (a) by removing ``540'' and adding in 
    its place ``526'', and in paragraph (b) by removing ``402(a)(2)(D)'' 
    and adding in its place ``402(a)(2)(c)(ii)''.
    
        Dated: September 8, 1999.
    Stephen F. Sundlof,
    Director, Center for Veterinary Medicine.
    [FR Doc. 99-24596 Filed 9-21-99; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Effective Date:
9/22/1999
Published:
09/22/1999
Department:
Food and Drug Administration
Entry Type:
Rule
Action:
Final rule; technical amendment.
Document Number:
99-24596
Dates:
September 22, 1999.
Pages:
51241-51241 (1 pages)
PDF File:
99-24596.pdf
CFR: (1)
21 CFR 510.105