[Federal Register: July 31, 2002 (Volume 67, Number 147)]
[Rules and Regulations]               
[Page 49568]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr31jy02-5]                         

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Parts 211, 226, 510, and 514

[Docket No. 88N-0038]
RIN 0910-AA02

 
Records and Reports Concerning Experience With Approved New 
Animal Drugs; Delay of Effective Date

AGENCY: Food and Drug Administration, HHS.

ACTION: Interim final rule; delay of effective date.

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SUMMARY: The Food and Drug Administration (FDA) is delaying the 
effective date of an interim final rule entitled ``Records and Reports 
Concerning Experience With Approved New Animal Drugs,'' published in 
the Federal Register of February 4, 2002 (67 FR 5046). The interim 
final rule amended FDA's regulations for records and reports concerning 
experience with approved new animal drugs, with an effective date of 
August 5, 2002. FDA is delaying the effective date so it can submit and 
seek approval on the information collection provisions of the rule 
under the Paperwork Reduction Act of 1995 and address comments received 
on the interim final rule.

DATES: The effective date published at 67 FR 5046, February 4, 2002, is 
delayed indefinitely. FDA will announce in the Federal Register an 
effective date.

FOR FURTHER INFORMATION CONTACT: Glenn Peterson, Center for Veterinary 
Medicine (HFV-212), Food and Drug Administration, 7500 Standish Pl., 
Rockville, MD 20855, 301-827-0224, or gpeterso@cvm.fda.gov.

    Dated: July 25, 2002.
Margaret M. Dotzel,
Associate Commissioner for Policy.
[FR Doc. 02-19299 Filed 7-30-02; 8:45 am]
BILLING CODE 4160-01-S