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FEDERAL REGISTER · NOTICEJuly 30, 2026NOTICE — NO LEGAL EFFECT

Animal Generic Drug User Fee Program Rates and Payment Procedures for Fiscal Year 2027

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Document details are published in the U.S. Federal Register; SPEQ surfaces them for reference and is not affiliated with or endorsed by the FDA or the Office of the Federal Register. The authoritative text is on federalregister.gov.

STATUSNOTICE — NO LEGAL EFFECT
EFFECTIVE—
COMMENTS CLOSEOct 1, 2026 · closed
APPLIES TO · SPEQ TAGDrugVeterinary
Document type
Notice
Agency
Health and Human Services Department
Published
July 30, 2026
Comments close
October 1, 2026
Document number
2026-15341
Docket
FDA-2026-N-7498
ABSTRACT

The Food and Drug Administration (FDA, the Agency, or we) is announcing the fee rates and payment procedures for fiscal year (FY) 2027 generic new animal drug program user fees. The Federal Food, Drug, and Cosmetic Act (FD&C Act), as amended by the Animal Generic Drug User Fee Amendments of 2023 (AGDUFA IV), authorizes FDA to collect user fees for certain abbreviated applications for generic new animal drugs, for certain generic new animal drug products, for certain sponsors of such abbreviated applications for generic new animal drugs and/or investigational submissions for generic new animal drugs (JINADs), and for certain submissions related to JINAD files. This notice establishes the fee rates for FY 2027.

Abstract as published in the Federal Register.

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