HR 1843 · 119th CongressIn Committeecongress.gov ↗

To amend the Federal Food, Drug, and Cosmetic Act to increase transparency in generic drug applications.

What this bill does

AI plain-language summary

This bill requires the Food and Drug Administration to tell companies that want to make generic drugs whether their drug is the same as the original brand-name drug. If the generic drug is not the same, the FDA must explain why. The FDA must also create or update guidance that explains how it decides whether generic drugs are the same as brand-name drugs.

Introduced

March 5, 2025

Policy Area

Health

Your Vote

Discussion (0)

Explain what is at stake in this bill.

Sign in to join the discussion.

No comments yet. Be the first.