Current Good Manufacturing Practice for Medicated Feeds

---
identifier: "/us/fr/2014-01299"
source: "fr"
legal_status: "authoritative_unofficial"
title: "Current Good Manufacturing Practice for Medicated Feeds"
title_number: 0
title_name: "Federal Register"
section_number: "2014-01299"
section_name: "Current Good Manufacturing Practice for Medicated Feeds"
positive_law: false
currency: "2014-01-23"
last_updated: "2014-01-23"
format_version: "1.1.0"
generator: "[email protected]"
agency: "Health and Human Services Department"
document_number: "2014-01299"
document_type: "rule"
publication_date: "2014-01-23"
agencies:
  - "Health and Human Services Department"
  - "Food and Drug Administration"
cfr_references:
  - "21 CFR Part 225"
fr_citation: "79 FR 3738"
fr_volume: 79
docket_ids:
  - "Docket No. FDA-2013-N-0002"
effective_date: "2014-01-23"
fr_action: "Final rule, correcting amendment."
---


#  [Amended]

**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.

**FOR FURTHER INFORMATION CONTACT:**

George K. Haibel, Center for Veterinary  Medicine (HFV-6), Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 240-276-9019, *[email protected].*

**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.

**List of Subjects in 21 CFR Part 225**

Animal drugs, Animal feeds, Labeling, Packaging and containers, Reporting and recordkeeping requirements.

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:

**21 CFR Part 225**

**PART 225—CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS**

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

**Authority:**

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

**21 CFR Part 225**

§ 225.1

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”.

Dated: January 16, 2014.

Leslie Kux,

Assistant Commissioner for Policy.