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H.R. 2058

FDA Deeming Authority Clarification Act of 2015

FDA Deeming Authority Clarification Act of 2015

This bill amends the Federal Food, Drug, and Cosmetic Act to revise premarket review and reporting requirements for products deemed by the Food and Drug Administration (FDA) to be tobacco products.

A product is not subject to premarket review by the FDA if it is introduced to market before that type of product is deemed a tobacco product.

A person introducing a tobacco product that is substantially similar to a marketed product less than 21 months after that type of product is deemed a tobacco product must submit a report to the FDA on the similar product not later than 21 months after that type of product is deemed a tobacco product. (A report is required at least 90 days prior to introduction of a tobacco product that is substantially similar to a marketed product if that type of product has been deemed a tobacco product for 21 months or more.)

Referred to the Subcommittee on Health.

Rep. Cole, Tom [R-OK-4](R-OK)Sponsor
77 cosponsors2 D75 R
77cosponsors1committees5actions5subjects
  1. Committee

    Referred to the Subcommittee on Health.

    Health Subcommittee
  2. IntroReferralH11100

    Referred to the House Committee on Energy and Commerce.

    Energy and Commerce Committee
  3. IntroReferralB00100

    Sponsor introductory remarks on measure. (CR E596)

  4. IntroReferralIntro-H

    Introduced in House

  5. IntroReferral1000

    Introduced in House

FDA Deeming Authority Clarification Act of 2015 — Informed