2025-07759Notice

FDA Seeks Approval for Generic Drug User Fee Paperwork Updates

Published Date: 5/5/2025

Notice

Summary

The FDA is asking for approval to collect info from companies that make generic drugs. This helps keep the Generic Drug User Fee Program running smoothly, making sure safe and affordable medicines reach you faster. If you’re a drug maker, get ready for some paperwork updates soon!

Analyzed Economic Effects

2 provisions identified: 1 benefits, 1 costs, 0 mixed.

Generic Drug Makers: New Paperwork

The FDA is asking OMB to approve collecting information from companies that make generic drugs. If you make generic medicines, expect paperwork updates and information requests to support the Generic Drug User Fee Program.

Keeps Generics Reaching Patients Faster

The FDA says the information collection helps keep the Generic Drug User Fee Program running smoothly so safe, affordable generic medicines reach patients faster. That could help consumers obtain generic medicines more quickly.

Your PRIA Score

Score Hidden

Personalized for You

How does this regulation affect your finances?

Sign up for a PRIA Policy Scan to see your personalized alignment score for this federal register document and every other regulation we track. We analyze your financial profile against policy provisions to show you exactly what matters to your wallet.

Free to start

Key Dates

Published Date
5/5/2025

Department and Agencies

Department
Independent Agency
Agency
Health and Human Services Department
Food and Drug Administration
Source: View HTML
Back to Federal Register

Take It Personal

Get Your Personalized Policy View

Start a Free Government Policy Watch to see how policy affects your household, then upgrade to PRIA Full Coverage for year-round monitoring.

Already have an account? Sign in