Increasing Prescription Drug Competition Act
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Increasing Prescription Drug Competition Act
This bill provides that certifications in generic drug applications of certain patents involved in Risk Evaluation and Mitigation Strategy (REMS) programs have no effect upon the drug's approval. (The Food and Drug Administration sometimes requires a REMS program for certain drugs with safety risks, which may include restrictions on a drug's distribution through elements to ensure safe use (ETASU), such as special requirements for pharmacies that dispense the drug.)
Specifically, certifications in generic drug applications with respect to patents that involve an ETASU for REMS requirements have no effect on the effective date of the drug's approval, notwithstanding any other provisions that allow for a stay of approval pending litigation outcomes (i.e., 30-month stay).
The bill also specifies that in a civil action alleging patent infringement with respect to REMS requirements, the sponsor of the approved brand-name drug may only seek damages from (rather than an injunction against) the generic drug applicant.
Referred to the Subcommittee on Health.
- Introduced in House Formatted Text PDF Formatted XML
Cite this page
U.S. Congress. (2026). H.R. 4692: Increasing Prescription Drug Competition Act. 118th Congress. Open America. https://openamerica.io/bill/118-HR-4692/
"H.R. 4692: Increasing Prescription Drug Competition Act." 118th Congress, 2026, Open America, https://openamerica.io/bill/118-HR-4692/.
H.R. 4692, 118th Cong. (2026), https://openamerica.io/bill/118-HR-4692/.
[H.R. 4692: Increasing Prescription Drug Competition Act](https://openamerica.io/bill/118-HR-4692/)