To provide for reconciliation pursuant to title II of H. Con. Res. 14.
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Last progress July 4, 2025 (7 months ago)
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Bipartisan Health Care Act
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Last progress March 6, 2025 (11 months ago)
Creates a federal system to measure and publish national average drug acquisition costs by running monthly surveys of retail and certain non‑retail pharmacies, requires pharmacies to respond, and funds an HHS Inspector General study. Changes Medicaid payment rules to ban ‘‘spread pricing’’ by requiring PBMs and similar entities to use transparent pass‑through pricing, disclose drug‑level costs, limit administrative fees to fair market value, and make spread pricing ineligible for Federal Medicaid matching funds. The bill includes civil penalties for noncompliance (up to $100,000 per violation), an appropriation of $5,000,000 for the IG study in FY2026, and implementation flexibilities for HHS (including exemptions from some notice-and-comment and paperwork rules). PBMs, pharmacies, States (Medicaid programs), and Medicaid beneficiaries are the main parties affected.
The Secretary of Health and Human Services shall conduct monthly surveys of retail community pharmacy drug prices and applicable non-retail pharmacy drug prices to determine national average drug acquisition cost benchmarks; the Secretary may contract with a vendor for these surveys.
A vendor used for the surveys must update the Secretary at least monthly on survey prices and must differentiate, when collecting and reporting cost information, whether a pharmacy is a retail community pharmacy or an applicable non-retail pharmacy and, for applicable non-retail pharmacies, which type it is (using pharmacy type indicators in Secretary guidance).
States must require any retail community pharmacy or applicable non-retail pharmacy that receives any payment, reimbursement, administrative fee, discount, rebate, or other price concession related to dispensing covered outpatient drugs for Medicaid beneficiaries to respond to the surveys.
The Secretary shall make information on national drug acquisition prices obtained under the surveys publicly available and include at least: the monthly survey response rate (with a list of pharmacies not in compliance), the sampling methodology and sample size each month, and information on price concessions to pharmacies to the extent that information can be publicly released.
The Secretary shall enforce survey requirements by establishing civil money penalties for retail community pharmacies and applicable non-retail pharmacies for refusing or failing to respond to survey requests, knowingly providing false information, or otherwise failing to comply.
Who is affected and how:
Pharmacies (retail community and defined non‑retail): Must respond to monthly HHS surveys about drug acquisition costs and provide data. For Medicaid‑covered dispensing pharmacies, they should receive pass‑through payments from PBMs instead of being paid a lower net amount if spread pricing had been used. Compliance creates administrative work and potential penalties for nonresponse.
Pharmacy Benefit Managers (PBMs) and contracted managed‑care or other entities: Must adopt transparent pass‑through contracts, disclose granular drug‑level costs and administrative fees, and limit administrative fees to fair market value. PBMs will likely lose a source of margin if they previously relied on spread pricing; they will face increased compliance, reporting, and potential revenue impacts.
State Governments and Medicaid programs: Must revise contracts and oversight to enforce pass‑through pricing and to require pharmacy participation in surveys. States will have new regulatory and administrative duties to implement changes and to collect and submit data; some costs to states may arise unless covered by federal support.
HHS and HHS Office of Inspector General: Gain new authorities to collect and publish pricing benchmarks, study survey data (with a $5M FY2026 appropriation), and oversee transparency of pricing. HHS is given expedited implementation powers (limited notice‑and‑comment and paperwork exemptions) which accelerate rule implementation but may invite scrutiny.
Medicaid beneficiaries and patients: Intended long‑term effect is greater price transparency and reduction of hidden middleman charges, which could improve pharmacy access or slow price growth. Short‑term effects depend on how PBMs, pharmacies, and States change contracts; there is a risk of transitional disruption in some local pharmacy networks.
Private sector implications: PBMs may see lower margins and challenge requirements legally or through contract adjustments; some smaller pharmacies may face reporting burdens but could benefit from more direct reimbursement. Insurers and managed care organizations could face higher visible drug costs on their books if PBM margins are eliminated, altering premium or rate dynamics.
Fiscal impact: The bill directs $5M to the OIG for FY2026 for the study; it also removes Federal matching funds for spread‑pricing payments, which may reduce some Federal outlays tied to spread pricing but could shift reported Medicaid spending. States will incur administrative costs to update contracts and enforcement procedures.
Potential risks and tradeoffs:
Last progress March 11, 2025 (11 months ago)
Introduced on March 11, 2025 by Peter Welch
Read twice and referred to the Committee on Finance.