Medicated Feed Mill License; Veterinary Feed Directive Drugs; Change of Address, 51966 [2024-13678]

Download as PDF 51966 Federal Register / Vol. 89, No. 120 / Friday, June 21, 2024 / Rules and Regulations AIRAC date 11–Jul–24 11–Jul–24 11–Jul–24 11–Jul–24 11–Jul–24 11–Jul–24 11–Jul–24 11–Jul–24 11–Jul–24 State City Airport name FDC date ..... ..... ..... ..... ..... ..... ..... ..... ..... NY NY NY MS MS CA OH IA FL Farmingdale ............ Farmingdale ............ Farmingdale ............ Clarksdale ............... Clarksdale ............... Sacramento ............ West Union ............. Iowa Falls ............... Tallahassee ............ Republic .................................. Republic .................................. Republic .................................. Fletcher Fld ............................. Fletcher Fld ............................. Sacramento Mather ................. Alexander Salamon ................. Iowa Falls Muni ....................... Tallahassee Intl ....................... 4/5157 4/5161 4/5163 4/5171 4/5188 4/5313 4/6917 4/8135 4/8813 5/16/2024 5/16/2024 5/16/2024 5/16/2024 5/16/2024 5/17/2024 5/20/2024 5/22/2024 5/24/2024 11–Jul–24 ..... 11–Jul–24 ..... 11–Jul–24 ..... CO NM NM Gunnison ................ Clovis ...................... Clovis ...................... Gunnison-Crested Butte Rgnl Clovis Rgnl .............................. Clovis Rgnl .............................. 4/8900 4/8942 4/9752 5/28/2024 5/28/2024 5/28/2024 [FR Doc. 2024–13507 Filed 6–20–24; 8:45 am] BILLING CODE 4910–13–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration (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 [Docket No. FDA–2024–N–2731] Administrative practice and procedure, Animal drugs, Confidential business information, Reporting and recordkeeping requirements. AGENCY: Food and Drug Administration, 21 CFR Part 558 HHS. Animal drugs, Animal feeds. Final rule; technical amendment. ACTION: 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 nonsubstantive. 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, Katherine.Collins@fda.hhs.gov. 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 SUMMARY: VerDate Sep<11>2014 16:17 Jun 20, 2024 Jkt 262001 Procedure name RNAV (RNP) Z RWY 14, Orig–B. ILS OR LOC RWY 14, Amdt 8G. RNAV (GPS) RWY 32, Amdt 1. RNAV (GPS) RWY 36, Amdt 2. RNAV (GPS) RWY 18, Amdt 2. RNAV (GPS) RWY 22R, Orig. RNAV (GPS) RWY 5, Orig–C. RNAV (GPS) RWY 13, Amdt 1A. ILS OR LOC RWY 27, ILS RWY 27 (CAT II), Amdt 10C. VOR OR GPS–A, Amdt 7D. RNAV (GPS) RWY 4, Amdt 1. RNAV (GPS) RWY 22, Amdt 1. PART 558—NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS 3. The authority citation for part 558 continues to read as follows: Authority: 21 U.S.C. 354, 360b, 360ccc, 360ccc–1, 371. 4. In § 558.6, revise paragraph (c)(7) to read as follows: 21 CFR Parts 515 and 558 Medicated Feed Mill License; Veterinary Feed Directive Drugs; Change of Address ddrumheller on DSK120RN23PROD with RULES1 FDC No. 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 1. The authority citation for part 515 continues to read as follows: ■ Authority: 21 U.S.C. 360b, 371. 2. In § 515.10, revise paragraphs (c) and (e) to read as follows: ■ § 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): MedicatedFeedsTeamMail@fda.hhs.gov. * * * * * 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 DEPARTMENT OF HOMELAND SECURITY Coast Guard § 515.10 Medicated feed mill license applications. 33 CFR Part 100 * [Docket Number USCG–2024–0169] * * * * (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): MedicatedFeedsTeamMail@fda.hhs.gov. * * * * * (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. PO 00000 Frm 00012 Fmt 4700 Sfmt 4700 RIN 1625–AA08 Special Local Regulation; Sail Grand Prix; Upper Bay, New York City, NY Coast Guard, DHS. Temporary final rule. AGENCY: ACTION: The Coast Guard is establishing a temporary special local regulation in the Upper Bay of New York Harbor in support of Sail Grand Prix 2024 from June 21, 2024, through June 23, 2024. This special local regulation is necessary to provide for SUMMARY: E:\FR\FM\21JNR1.SGM 21JNR1

Agencies

[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.

-----------------------------------------------------------------------

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

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