HRES 161
113th Congress
House
Expressing the sense of the House of Representatives that the Food and Drug Administration should encourage the use of abuse-deterrent formulations of drugs.
Health
Drug safety, medical device, and laboratory regulationDrug, alcohol, tobacco usePrescription drugs
Everywhere this bill has been
3 steps
Introduced
In committee
Reported out
Agreed to (House)
Apr 19, 2013
Referred to the Subcommittee on Health.
Apr 15, 2013
Referred to the House Committee on Energy and Commerce.
Apr 15, 2013
Introduced in House
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Latest action
Referred to the Subcommittee on Health.
Plain-English 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.
Related & companion bills
1
Bill text
1 version
- Introduced in House Formatted Text PDF Formatted XML
Committees of jurisdiction
2
Cite this page
U.S. Congress. (2026). 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.. 113th Congress. Open America. https://openamerica.io/bill/113-HRES-161/
"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.." 113th Congress, 2026, Open America, https://openamerica.io/bill/113-HRES-161/.
H. Res. 161, 113th Cong. (2026), https://openamerica.io/bill/113-HRES-161/.
[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.](https://openamerica.io/bill/113-HRES-161/)