02-19299. Records and Reports Concerning Experience With Approved New Animal Drugs; Delay of Effective Date
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Start Preamble
AGENCY:
Food and Drug Administration, HHS.
ACTION:
Interim final rule; delay of effective date.
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.
Start Further InfoFOR 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.
End Further Info Start SignatureDated: 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
Document Information
- Effective Date:
- 2/4/2002
- Published:
- 07/31/2002
- Department:
- Food and Drug Administration
- Entry Type:
- Rule
- Action:
- Interim final rule; delay of effective date.
- Document Number:
- 02-19299
- 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.
- Pages:
- 49568-49568 (1 pages)
- Docket Numbers:
- Docket No. 88N-0038
- RINs:
- 0910-AA02: New Animal Drug Approval Process; Implementation of Title I of the Generic Animal Drug and Patent Term Restoration Act (GADPTRA)
- RIN Links:
- https://www.federalregister.gov/regulations/0910-AA02/new-animal-drug-approval-process-implementation-of-title-i-of-the-generic-animal-drug-and-patent-ter
- PDF File:
- 02-19299.pdf
- CFR: (4)
- 21 CFR 211
- 21 CFR 226
- 21 CFR 510
- 21 CFR 514