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HF4140 • 2026

Minnesota Community Pharmacy Patient Access and Fair Reimbursement Act established, and rulemaking required.

Minnesota Community Pharmacy Patient Access and Fair Reimbursement Act established, and rulemaking required.

Passed Legislature

This bill passed both chambers and reached final enrollment, even if later executive action is not shown here.

Sponsor
Reyer, Bierman
Last action
2026-03-09
Official status
Introduction and first reading, referred to Health Finance and Policy
Effective date
Not listed

Plain English Breakdown

The plain English breakdown is still being put together. The official documents below are already here.

Bill History

  1. 2026-03-09 House

    Introduction and first reading, referred to Health Finance and Policy

Official Summary Text

Minnesota Community Pharmacy Patient Access and Fair Reimbursement Act established, and rulemaking required.

Current Bill Text

Read the full stored bill text
A bill for an act

relating to health; establishing the Minnesota Community Pharmacy Patient Access

and Fair Reimbursement Act; requiring rulemaking; proposing coding for new

law in Minnesota Statutes, chapter 62J.

BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF MINNESOTA:

Section 1.

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[62J.901] MINNESOTA COMMUNITY PHARMACY PATIENT ACCESS

AND FAIR REIMBURSEMENT ACT.

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Subdivision 1.

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Title.

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This section shall be known as the "Minnesota Community

Pharmacy Patient Access and Fair Reimbursement Act."

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Subd. 2.

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Scope.

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This section is intended to protect patients' access to community

pharmacies by ensuring sustainable reimbursement rates for community pharmacies and to

prevent unfair reimbursement practices that cause pharmacy closures, thereby safeguarding

patient access to essential pharmaceutical care and maintaining a strong community health

infrastructure across the state. This section regulates pharmacy benefit manager conduct

and reimbursement practices and does not alter health plan benefit design or federal program

requirements.

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Subd. 3.

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Definitions.

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(a) For purposes of this section, the following terms have the

meanings given.

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(b) "Community pharmacy" means an outpatient retail pharmacy licensed under chapter

151 that is not owned, operated, managed, or controlled, either directly or indirectly, through

an affiliate or subsidiary by a:

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(1) pharmacy benefit manager licensed under chapter 62W;

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(2) health carrier, as defined in section 62A.011, subdivision 2;

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(3) government entity;

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(4) mail-order pharmacy; or

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(5) specialty pharmacy.

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(c) "National Average Drug Acquisition Cost" or "NADAC" means the publicly available,

federally established benchmark reflecting the average acquisition cost of outpatient

prescription drugs purchased by retail community pharmacies, as determined by the Centers

for Medicare and Medicaid Services.

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(d) "Pharmacy benefit manager" or "PBM" has the meaning given in section 62W.02,

subdivision 15.

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(e) "Pharmacy reimbursement ceiling" means the maximum reimbursement rate for

prescription drugs dispensed by a pharmacy established under subdivision 4.

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(f) "Professional dispensing fee" means the fee paid to a pharmacy for the cost of

dispensing a medication, excluding the cost of the drug itself. The fee is intended to cover

the professional services provided by the pharmacy dispensing the medication, in accordance

with section 256B.0625, subdivision 13e.

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(g) "Wholesale acquisition cost" or "WAC" means the manufacturer's list price for a

prescription drug to wholesalers or direct purchasers in the United States, not including any

discounts, rebates, or other price concessions.

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Subd. 4.

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Fair pharmacy reimbursement.

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(a) Except as provided in paragraph (c), this

subdivision applies to prescription drugs dispensed by a community pharmacy, as defined

in subdivision 3, and to claims adjudicated by a PBM under a health plan or pharmacy

benefit plan.

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(b) To improve patient access to pharmacy services and support the financial viability

of community pharmacies, for any prescription drug dispensed by a community pharmacy

and for any claim adjudicated by a PBM to which this subdivision applies, the total

reimbursement to the community pharmacy must be equal to:

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(1) the NADAC for the drug on the day of claim adjudication or, if the NADAC is

unavailable, the WAC for that drug on the day of claim adjudication, plus an additional

amount equal to four percent of the calculated total ingredient cost as derived from the

applicable NADAC or WAC amount, or $50, whichever is less; and

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(2) a professional dispensing fee as specified in section 256B.0625, subdivision 13e,

which must be equal to the professional dispensing fee paid by the state under the medical

assistance program and adjusted biennially based on an independent cost-of-dispensing

survey reflecting inflation, labor costs, and operational expenses.

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(c) The reimbursement standard established in this subdivision constitutes both the

minimum and maximum reimbursement amount for purposes of this section and may not

be altered by contract, network design, or other reimbursement methodology.

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Subd. 5.

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Scope of application; covered entities; exclusions.

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(a) Nothing in this section

requires reimbursement at or above NADAC or WAC for drugs purchased under the federal

340B Drug Pricing Program. Reimbursement for drugs purchased under the 340B program

must comply with applicable state and federal law.

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(b) This section does not apply to claims paid under Medicare or Medicaid, including

claims paid under Medicare Part B, Medicare Part D, and Medicaid fee-for-service or

managed care, or under any other state or federal program for which reimbursement is

established by statute, regulation, state plan, contract approved by a federal agency, or

federal waiver.

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(c) This section regulates the reimbursement practices of pharmacy benefit managers

licensed under chapter 62W with respect to claims paid under commercial health plans and

pharmacy benefit plans subject to state regulation.

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Subd. 6.

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Prohibition on below-cost and postclaim manipulation.

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(a) A PBM must

not reimburse a community pharmacy in an amount below the reimbursement standard

established in this section.

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(b) A PBM must not impose any fee, adjustment, recoupment, reconciliation payment,

performance metric, direct or indirect remuneration fee, or other mechanism that results in

a community pharmacy receiving less than the total reimbursement required under this

section.

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Subd. 7.

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Ban on spread pricing.

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PBMs are prohibited from engaging in spread pricing

in commercial and state-regulated plans. A PBM may not retain any portion of payments

made by a health plan, insurer, government program, or other payer beyond the amount

paid to the dispensing pharmacy, less enrollee cost sharing. PBMs must remit to the

dispensing pharmacy 100 percent of payments received, less patient cost-sharing.

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Subd. 8.

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Prohibition of retroactive claim denials.

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PBMs must not retroactively deny

or reduce claim reimbursement except in cases of fraud, billing errors, or documented

overpayment verified through an audit.

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Subd. 9.

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Prohibition on patient steering.

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PBMs must not require, coerce, steer, or

financially penalize an enrollee to use a PBM-owned, affiliated, or mail-order pharmacy.

A PBM must not impose higher cost-sharing, reduced benefits, or other financial or

administrative disadvantages on an enrollee who chooses to obtain prescription drugs from

a community pharmacy.

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Subd. 10.

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Enforcement and penalties.

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(a) The Department of Commerce has exclusive

authority to administer and enforce this section.

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(b) A community pharmacy, health carrier, plan sponsor, or enrollee may file a complaint

with the commissioner alleging a violation of this section. The commissioner shall investigate

alleged violations and may require the submission of claims data, pricing files, contracts,

and any other records necessary to determine compliance.

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(c) To ensure compliance with this section, the commissioner may:

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(1) conduct investigations and compel the production of unredacted records, pricing

agreements, claims data, contracts, and internal communications relevant to reimbursement

practices;

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(2) order corrective action including restitution, cease-and-desist orders, and prospective

pricing adjustments to remedy and prevent violations;

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(3) require annual compliance certification from PBMs attesting to full compliance with

this section. A false certification is subject to civil penalties and potential suspension of

licensure; and

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(4) publish an annual compliance report summarizing:

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(i) the number of violations identified;

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(ii) the amount of fines and restitution collected; and

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(iii) the impact on community pharmacy access and closures.

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(d) A PBM found to be reimbursing below the reimbursement standard established in

subdivision 4 is subject to a civil penalty of $5,000 per violation per claim. Repeat violations

are subject to escalating penalties of up to $20,000 per claim, not to exceed $2,000,000 per

enforcement action. The Department of Commerce may impose additional sanctions,

including suspension or revocation of a PBM's license to operate in the state.

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(e) If the commissioner determines that a PBM has violated this section, the commissioner

may:

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(1) order full restitution to the affected pharmacy, including interest and reasonable costs

incurred in the administrative proceeding; and

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(2) impose any additional sanctions authorized under this section.

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(f) A pharmacist or other individual who, in good faith, reports noncompliance, fraudulent

reimbursement practices, or retaliatory conduct by a PBM is protected from retaliation. The

commissioner shall establish a secure and confidential process for receiving reports. Verified

violations may result in additional penalties or corrective action.

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(g) A final order of the commissioner is subject to judicial review under chapter 14.

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Subd. 11.

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Rulemaking.

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The commissioner of commerce shall adopt necessary rules to

implement this section.

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Subd. 12.

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Severability.

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If any provision of this section or its application to any person

or circumstance is held invalid, the invalidity does not affect other provisions or applications

of the section that can be given effect without the invalid provision or application.

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EFFECTIVE DATE.

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This section is effective July 1, 2026.

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