Expresses the sense of the Senate 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 recognized by FDA as effective, and (2) require generic versions of abuse-deterrent opioid products to be formulated with comparable abuse-deterrent features.
Referred to the Subcommittee on Health.
Introduced in Senate
Referred to the Committee on Health, Education, Labor, and Pensions. (text of measure as introduced: CR S2654)
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