[Federal Register Volume 59, Number 218 (Monday, November 14, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-27924]
[[Page Unknown]]
[Federal Register: November 14, 1994]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 520
Oral Dosage Form New Animal Drugs; Oxytetracycline Hydrochloride
Soluble Powder; Correction
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule; correction.
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SUMMARY: The Food and Drug Administration (FDA) is correcting a final
rule that appeared in the Federal Register of August 15, 1994 (59 FR
41664). The document amended the animal drug regulations to reflect
approval of an abbreviated new animal drug application (ANADA 200-066)
filed by Agri Laboratories, Ltd. The regulation was published with an
inadvertent error in the amendatory language. This document corrects
that error.
EFFECTIVE DATE: August 15, 1994.
FOR FURTHER INFORMATION CONTACT: John W. Borders, Center for Veterinary
Medicine (HFV-238), Food and Drug Administration, 7500 Standish Pl.,
Rockville, MD 20855, 301-594-1737.
SUPPLEMENTARY INFORMATION: In FR Doc. 94-19934, appearing on page 41664
in the Federal Register of August 15, 1994, the following correction is
made: On page 41664, in the third column, amendatory instruction number
2 is corrected to read: ``Section 520.1660d is amended by adding new
paragraphs (a)(6) and (b)(4), and by revising the next to last sentence
in paragraphs (e)(1)(ii)(A)(3), (e)(1)(ii)(B)(3), and (e)(1)(ii)(C)(3),
and the last sentence in paragraph (e)(1)(iii)(C) to read as
follows:''.
Dated: November 3, 1994.
Stephen F. Sundlof,
Director, Center for Veterinary Medicine.
[FR Doc. 94-27924 Filed 11-10-94; 8:45 am]
BILLING CODE 4160-01-F