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Protects Generic Drug Approvals
Recent Bills/Protects Generic Drug Approvals

Protects Generic Drug Approvals

IntroducedN/A
Introduced1 year ago
Intro
Senate
House
Pres
Read twice and referred to the Committee on the Judiciary.
Why This Matters

This bill creates protections for generic drug manufacturers, allowing them to seek approval without violating certain patents related to drug use.

If you rely on generic medications, this bill could help lower prices by making it easier for companies to get approved.
Who this affects
generic drug manufacturers · consumers seeking affordable medications
What changes is this bill making?
  1. 1This bill allows generic drug companies to apply for approval without infringing on certain patents.
  2. 2It specifically targets method of use patents for drugs and biological products.
  3. 3The bill encourages competition in the pharmaceutical market, potentially lowering drug prices.
  4. 4It provides a legal safe harbor for companies promoting their products under approved labels.
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
Senate
House
Pres
IntroducedCurrentJan 9, 2025

Read twice and referred to the Committee on the Judiciary.

Sponsors
See all 4 sponsors
Senate
House
President

The President

Joe Biden
46th President
Awaiting Vote
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