H.R. 6485 Introduced Commerce

Skinny Labels, Big Savings Act

To amend title 35, United States Code, to provide for a safe harbor from infringement of a method of use patent relating to drugs or biological products.

  1. Introduced
  2. Committee
  3. Passed House
  4. Passed Senate
  5. To President
  6. Became law
Sponsor Rep. Cline, Ben [R-VA-6] Introduced December 5, 2025 Cosponsors 6 (3 D, 3 R) Latest action December 5, 2025

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 GlaxoSmithKline 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; or
- describing 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.

Summary by the Congressional Research Service, Library of Congress.

Congress.gov

Actions

  1. Dec 5, 2025 Referred to the House Committee on the Judiciary.
  2. Dec 5, 2025 Introduced in House

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