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Drug Patent Protection Bill
Recent Bills/Drug Patent Protection Bill

Drug Patent Protection Bill

IntroducedDecember 5, 2025
Introduced8 months ago
Intro
House
Senate
Pres
Introduced in House
Why This Matters

The Skinny Labels, Big Savings Act allows companies to develop and market generic drugs without violating certain patents. This change aims to increase competition and lower drug prices for consumers.

If you need medications, this bill could help lower your costs by increasing competition among drug manufacturers.
Who this affects
Patients needing medications · Generic drug manufacturers
What changes is this bill making?
  1. 1This bill provides legal protection for certain drug patents.
  2. 2It allows companies to seek approval for generic drugs without infringing on patents.
  3. 3The bill promotes competition in the drug market by easing restrictions.
  4. 4It helps lower the cost of medications for consumers.
  5. 5The bill applies to both drugs and biological products.
Read the detailed summary

Skinny Labels, Big Savings Act This bill provides a statutory safe harbor from patent infringement claims for generic or biosimilar manufacturers that seek or obtain approval for skinny labels of their drugs. Under current law, the Food and Drug Administration (FDA) may approve generic and biosimilar drugs through a process known as skinny labeling, which allows a generic manufacturer to seek approval only for approved uses of the drug that are no longer protected by patents. However, in Glaxo Smith Kline LLC v. Teva Pharmaceuticals USA, Inc., a court held that a generic manufacturer may sometimes be liable for patent infringement when it markets skinny label generics. The bill specifically lists the following as actions that are not considered infringement of a method of use claim in a patent under the Federal Food, Drug, and Cosmetic Act:submitting or seeking approval of a skinny label for a generic or biosimilar drug; promoting or commercially marketing a drug with skinny labeling approved by the FDA; ordescribing a drug product approved by the FDA as a generic of, or therapeutically equivalent to, the branded drug. The bill also applies the safe harbor to similar actions under the Public Health Service Act.

Bill Progress1 of 4
Bills must pass the House, Senate, and be signed by the President to become law.
Intro
House
Senate
Pres
IntroducedCurrentDec 5, 2025

Introduced in House

Sponsors
See all 2 sponsors
House
Senate
President

The President

Donald Trump
President
Awaiting Vote
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