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Rule

New Animal Drugs for Use in Animal Feeds; Chlortetracycline

A Rule by the Food and Drug Administration on 12/30/2004

Document Details

Information about this document as published in the Federal Register.

Printed version:
PDF
Publication Date:
12/30/2004
Agencies:
Food and Drug Administration
Dates:
This rule is effective December 30, 2004.
Effective Date:
12/30/2004
Document Type:
Rule
Document Citation:
69 FR 78305
Page:
78305-78306 (2 pages)
CFR:
21 CFR 558
Document Number:
04-28578
Document Details
Published Document

This document has been published in the Federal Register. Use the PDF linked in the document sidebar for the official electronic format.

Start Preamble

AGENCY:

Food and Drug Administration, HHS.

ACTION:

Final rule, technical amendment.

SUMMARY:

The Food and Drug Administration (FDA) is amending the animal drug regulations to add the approved withdrawal time to the limitations to conditions of use for chlortetracycline Type C medicated feeds for chickens when fed at the 500 gram per ton level. This change is being made to improve the accuracy of the regulations.

DATES:

This rule is effective December 30, 2004.

Start Further Info

FOR FURTHER INFORMATION CONTACT:

George K. Haibel, Center for Veterinary Medicine (HFV- 6), Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 301-827-4567, e-mail: george.haibel@fda.gov.

End Further Info End Preamble Start Supplemental Information

SUPPLEMENTARY INFORMATION:

FDA has found that the April 1, 2004, edition of Title 21, Parts 500 to 599 of the Code of Federal Regulations (CFR) does not reflect the approved withdrawal time for chlortetracycline in Type C medicated feeds for chickens when fed at the 500 gram per ton level. The approved 24-hour withdrawal time at this dose level was inadvertently removed for all sponsors at the time of a supplemental approval of a zero-day withdrawal time for AUREOMYCIN Type C medicated chicken feeds under NADA 48-761 (63 FR 57245 at 57247, October 27, 1998). At this time, FDA is amending the regulations to correct this error in 21 CFR 558.128. This action is being taken to improve the accuracy of the regulations.

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.

Start List of Subjects

List of Subjects in 21 CFR Part 558

End List of Subjects Start Amendment Part

Therefore, under the Federal Food, Drug, and Cosmetic Act and under authority delegated to the Commissioner of Food and Drugs and redelegated to the Center for Veterinary Medicine,

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PART 558—NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS

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1. The authority citation for

End Amendment Part Start Authority

Authority: 21 U.S.C. 360b, 371.

End Authority Start Amendment Part

2. Section 558.128 is amended by revising paragraph (e)(1)(iv) to read as follows:

End Amendment Part
Chlortetracycline.
* * * * *

(e) * * *

(1) * * *

Chlortetracycline amountIndications for useLimitationsSponsor
*         *         *         *         *         *         *
(iv) 500 g/tonChickens: For the reduction of mortality due to E. coli infections susceptible to chlortetracycline.1. Feed for 5 d; 0-day withdrawal time when formulated from AUREOMYCIN Type A medicated articles or Type B medicated feeds under NADA 48-761. 2. Feed for 5 d; withdraw 24 h prior to slaughter; do not feed to chickens producing eggs for human consumption.046573
   017519, 046573, 048164, 066104
*         *         *         *         *         *         *
Start Printed Page 78306
* * * * *
Start Signature

Dated: December 16, 2004.

Steven D. Vaughn,

Director, Office of New Animal Drug Evaluation, Center for Veterinary Medicine.

End Signature End Supplemental Information

[FR Doc. 04-28578 Filed 12-29-04; 8:45 am]

BILLING CODE 4160-01-S

Published Document