FDA Announces FY 2025 Animal Drug User Fee Rates for ADUFA and AGDUFA

July 31, 2024

The U.S. Food and Drug Administration has announced in the Federal Register the fiscal year (FY) 2025 fee rates and payment procedures for animal drugs subject to user fees under the Animal Drug and Animal Generic Drug User Fee Amendments of 2023.

The Animal Drug User Fee Act (ADUFA), originally signed into law in 2003 and reauthorized in 2008, 2013, 2018 and 2023, authorizes the FDA to collect user fees for certain animal drug applications and supplemental applications, products, establishments, and sponsors of animal drug applications and/or investigational animal drug submissions. These resources supplement funding provided by Congressional budget authority to enhance the performance of the drug review process ensuring that new animal drug products are safe and effective for animals, and that food derived from treated animals will be safe for consumption. ADUFA V reauthorizes the FDA to collect user fees through FY 2028.

The Animal Generic Drug User Fee Act (AGDUFA), originally signed into law in 2008 and reauthorized in 2013, 2018 and 2023, was designed to supplement the Congressional budget authority to enhance the performance of the generic new animal drug review process, which enables the FDA to ensure that generic new animal drug products are safe and effective. AGDUFA IV reauthorizes the FDA to collect user fees for certain abbreviated applications for generic new animal drugs, generic investigational new animal drug files, generic new animal drug products, and from certain sponsors of abbreviated applications for generic new animal drugs and/or investigational submissions for generic new animal drugs. The user fees for sponsors are prorated based on the number of approved abbreviated applications the sponsor currently holds. AGDUFA IV reauthorizes the FDA to collect user fees through FY 2028.

In the period since Congress first passed ADUFA in 2003 until July 26, 2024, the FDA has approved 536 new animal drugs -- both original approvals and major enhancements to these approvals (e.g., new indications, new species). In the period since AGDUFA was passed in 2008 until July 26, 2024, the FDA has approved 374 generic new animal drugs.

The tables below reflect the ADUFA V and AGDUFA IV fee rates for FY 2025.

ADUFA V FY 2025 Fees

Animal Drug User Fee Category	Fee Rate for FY 2025
Animal Drug Application Fees: Animal Drug Application Supplemental Animal Drug Application requiring safety or effectiveness data and Animal Drug Application subject to criteria in 21 U.S.C. 360b(d)(4)) (50% of application fee)	$581,735 $290,867
Product Fee	$10,705
Establishment Fee	$157,702
Sponsor Fee	$137,446

AGDUFA IV FY 2025 Fees

Generic New Animal Drug User Fee Category	Fee Rate for FY 2025
Abbreviated Application for a Generic New Animal Drug (except those subject to criteria in 21 U.S.C. 360b(d)(4))	$161,907
Abbreviated Application for a Generic New Animal Drug subject to criteria in 21 U.S.C. 360b(d)(4) (50% of application fee)	$80,954
Generic Investigational New Animal Drug File Fee (JINAD)	$50,000
Product Fee	$16,139
Sponsor Fee 100% (holds > 6 approved abbreviated applications) 75% (holds 2-6 approved abbreviated applications) 50% (holds 0-1 approved abbreviated applications)	$270,204 $202,653 $135,102

In addition to announcing the ADUFA and AGDUFA user fee rates for FY 2025 and explaining how such rates were calculated, the Federal Register notices also provide details on how to submit payment of these fees to the FDA. The application fee rates are effective for applications received by the FDA’s Center for Veterinary Medicine from October 1, 2024, until September 30, 2025. The FDA will issue invoices for FY 2025 product, establishment, and sponsor fees by December 31, 2024, and payment will be due by January 31, 2025. The FDA will not accept an application for filing unless the FDA has received payment for all fees due from the sponsor.

For additional information regarding the financials and performance of ADUFA and AGDUFA, we have included a link for the FY 2023 Financial and Performance Reports below.

For more information, contact Lisa Kable at Lisa.Kable@fda.hhs.gov. Please send general questions concerning ADUFA to cvmadufa@fda.hhs.gov and questions concerning AGDUFA to cvmagdufa@fda.hhs.gov.

Additional Information:

Issued by FDA Center for Veterinary Medicine.
For questions, Contact CVM.