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Rule

Current Good Manufacturing Practice for Medicated Feeds

Document Details

Information about this document as published in the Federal Register.

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AGENCY:

Food and Drug Administration, HHS.

ACTION:

Final rule, correcting amendment.

SUMMARY:

The Food and Drug Administration (FDA) is amending the regulations for good manufacturing practice of animal feeds containing a new animal drug to correctly cite the applicable section of the Federal Food, Drug, and Cosmetic Act (FD&C Act). This action is being taken to improve the accuracy of the regulations.

DATES:

This rule is effective January 23, 2014.

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FOR FURTHER INFORMATION CONTACT:

George K. Haibel, Center for Veterinary Start Printed Page 3739Medicine (HFV-6), Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 240-276-9019, ghaibel@fda.hhs.gov.

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SUPPLEMENTARY INFORMATION:

FDA has noticed the regulations for good manufacturing practice of animal feeds containing a new animal drug do not correctly cite the applicable section of the FD&C Act. At this time, FDA is making a correcting amendment in 21 CFR 225.1. This action is being taken to improve the accuracy of the regulations.

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List of Subjects in 21 CFR Part 225

  • Animal drugs
  • Animal feeds
  • Labeling
  • Packaging and containers
  • Reporting and recordkeeping requirements
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Therefore, under the Federal Food, Drug, and Cosmetic Act and under authority delegated to the Commissioner of Food and Drugs, 21 CFR part 225 is amended as follows:

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PART 225—CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS

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1. The authority citation for 21 CFR part 225 continues to read as follows:

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Authority: 21 U.S.C. 351, 352, 360b, 371, 374.

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[Amended]
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2. In § 225.1, in the last sentence in paragraph (b)(1), remove “section 402(a)(2)(D) of the act” and in its place add “section 402(a)(2)(C)(ii) of the act”.

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Dated: January 16, 2014.

Leslie Kux,

Assistant Commissioner for Policy.

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[FR Doc. 2014-01299 Filed 1-22-14; 8:45 am]

BILLING CODE 4160-01-P