[Federal Register Volume 62, Number 37 (Tuesday, February 25, 1997)]
[Rules and Regulations]
[Page 8370]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 97-4518]


=======================================================================
-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 520


Oral Dosage Form New Animal Drugs; Monensin Blocks; Correction

AGENCY: Food and Drug Administration, HHS.

ACTION: Final rule; correction.

-----------------------------------------------------------------------

SUMMARY: The Food and Drug Administration (FDA) is correcting a final 
rule that appeared in the Federal Register of October 15, 1996 (61 FR 
53614). The document amended the animal drug regulations to reflect 
approval of supplemental new animal drug applications filed by 
Cooperative Research Farms and PM Ag Products, Inc. The document was 
published with an incorrect approval date. This document corrects that 
error.

EFFECTIVE DATE: October 15, 1996.

FOR FURTHER INFORMATION CONTACT: David L. Gordon, Center for Veterinary 
Medicine (HFV-238), Food and Drug Administration, 7500 Standish Pl., 
Rockville, MD 20855, 301-594-1737.

    In FR Doc. 96-26374, appearing on page 53614, in the Federal 
Register of Tuesday, October 15, 1996, the following correction is 
made:
    1. On page 53615, in the first column under the ``SUPPLEMENTARY 
INFORMATION'' caption, in line 14, ``September 10, 1996'' is corrected 
to read ``October 15, 1996''.

    Dated: February 10, 1997.
Robert C. Livingston,
Director, Office of New Animal Drug Evaluation, Center for Veterinary 
Medicine.
[FR Doc. 97-4518 Filed 2-24-97; 8:45 am]
BILLING CODE 4160-01-F