[Federal Register Volume 89, Number 120 (Friday, June 21, 2024)]
[Rules and Regulations]
[Page 51966]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-13678]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Parts 515 and 558

[Docket No. FDA-2024-N-2731]


Medicated Feed Mill License; Veterinary Feed Directive Drugs; 
Change of Address

AGENCY: Food and Drug Administration, HHS.

ACTION: Final rule; technical amendment.

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SUMMARY: The Food and Drug Administration (FDA or the Agency) is 
amending the regulations for medicated feed mill applications and for 
veterinary feed directive drugs to update addresses and simplify 
notification procedures. These technical amendments are being made to 
improve the accuracy of the Agency's regulations and are non-
substantive.

DATES: This rule is effective June 21, 2024.

FOR FURTHER INFORMATION CONTACT: Katherine Collins, Center for 
Veterinary Medicine, Food and Drug Administration, 7500 Standish Pl., 
Rockville, MD 20855, 301-796-6736, [email protected].

SUPPLEMENTARY INFORMATION: FDA is amending the animal drug regulations 
for medicated feed mill notification applications at 21 CFR 515.10 and 
for veterinary feed directive drugs at 21 CFR 558.6 to update addresses 
and Agency notification procedure. These technical amendments are being 
made to improve the accuracy of the Agency's regulations and are non-
substantive.
    Publication of this document constitutes final action on the 
changes under the Administrative Procedure Act (5 U.S.C. 553). FDA has 
determined that notice and public comment are unnecessary because this 
amendment to the regulations provides only technical or non-
substantive, ministerial changes to update addresses and Agency 
notification procedure.

List of Subjects

21 CFR Part 515

    Administrative practice and procedure, Animal drugs, Confidential 
business information, Reporting and recordkeeping requirements.

21 CFR Part 558

    Animal drugs, Animal feeds.

    Therefore, under the Federal Food, Drug, and Cosmetic Act and under 
authority delegated to the Commissioner of Food and Drugs, 21 CFR parts 
515 and 558 are amended as follows:

PART 515--MEDICATED FEED MILL LICENSE

0
1. The authority citation for part 515 continues to read as follows:

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


0
2. In Sec.  515.10, revise paragraphs (c) and (e) to read as follows:


Sec.  515.10  Medicated feed mill license applications.

* * * * *
    (c) Applications must be completed, signed, and submitted to the 
Food and Drug Administration, Center for Veterinary Medicine, Division 
of Food Compliance, 12225 Wilkins Ave., Rockville, MD 20852, or email 
(via attachment): [email protected].
* * * * *
    (e) Upon approval, the application will be signed by an authorized 
employee of FDA designated by the Commissioner of Food and Drugs, and a 
copy will be returned to the applicant.

PART 558--NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS

0
3. The authority citation for part 558 continues to read as follows:

    Authority: 21 U.S.C. 354, 360b, 360ccc, 360ccc-1, 371.


0
4. In Sec.  558.6, revise paragraph (c)(7) to read as follows:


Sec.  558.6  Veterinary feed directive drugs.

* * * * *
    (c) * * *
    (7) The notifications cited in paragraphs (c)(5) and (6) of this 
section must be submitted to the Food and Drug Administration, Center 
for Veterinary Medicine, Division of Food Compliance, 12225 Wilkins 
Ave., Rockville, MD 20852, or email (via attachment): 
[email protected].
* * * * *

    Dated: June 17, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2024-13678 Filed 6-20-24; 8:45 am]
BILLING CODE 4164-01-P