H.RES.161: Expressing the sense of the House of Representatives that the Food and Drug Administration should encourage the use of abuse-deterrent formulations of drugs.

About This Bill

  • This bill was introduced in the 113th Congress
  • This bill is primarily about health
  • Introduced April 15, 2013
  • Latest Major Action April 19, 2013

Bill Summary

Expresses the sense of the House of Representatives that the Food and Drug Administration (FDA) should exercise its acknowledged authority to: (1) refuse to approve generic versions of non-abuse-deterrent opioid products that have been replaced in the market with abuse-deterrent formulations, and (2) require generic versions of abuse-deterrent opioid products to be formulated with comparable abuse-deterrent features.

(Source: Library of Congress)

Bill Actions

Date Description
April 19, 2013
Referred to the Subcommittee on Health.
April 15, 2013
Referred to the House Committee on Energy and Commerce.
April 15, 2013

Introduced in the House by Harold Rogers (R-Ky.)

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