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Kentucky · Snapshot 09/05/2026

KRS 304.17A-595: Definitions for section -- Requirements for contract for provision of

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Where this section sits in the code

    pharmacy services -- Minimum reimbursements -- Administrative regulations.

    (1) As used in this section:

    (a) "Actual overpayment" means the portion of any amount p aid for pharmacy or

    pharmacist services that:

    1. Is duplicative because the pharmacy or pharmacist has already been paid

    for the services; or

    2. Was erroneously paid because the services were not rendered in

    accordance with the prescriber's order, in which case only the amount

    paid for that portion of the prescription that was filled incorrectly or in

    excess of the prescriber's order may be deemed an actual overpayment.

    The amount denied, refunded, or recouped shall not include the

    dispensing fee paid to th e pharmacy if the correct medication was

    dispensed to the patient;

    (b) "Ambulatory pharmacy" means a pharmacy that:

    1. Is open to the general public; and

    2. Dispenses outpatient prescription drugs;

    (c) "National average drug acquisition cost" means the nat ional average drug

    acquisition cost, or NADAC, for a prescription drug or other service that is:

    1. Determined by a survey of retail pharmacies; and

    2. Published by the federal Centers for Medicare and Medicaid Services;

    (d) "National drug code number" means the unique national drug code number

    that identifies a specific approved drug, its manufacturer, and its package

    presentation;

    (e) "Net amount" means the amount paid to the pharmacy or pharmacist by the

    insurer, pharmacy benefit manager, or other administrator less any fees, price

    concessions, and all other revenue passing from the pharmacy or pharmacist

    to the insurer, pharmacy benefit manager, or other administrator; and

    (f) "Wholesale acquisition cost" means the manufacturer's list price for the drug

    to wholesalers or direct purchasers in the United States, not including prompt

    pay or other discounts, rebates, or reductions in price, for the most rec ent

    month for which the information is available, as reported in wholesale price

    guides or other publications of drug pricing data.

    (2) To the extent permitted under federal law, every contract between a pharmacy or

    pharmacist and an insurer, a pharmacy be nefit manager, or any other administrator

    of pharmacy benefits for the provision of pharmacy or pharmacist services under a

    health plan, either directly or through a pharmacy services administration

    organization or group purchasing organization, shall:

    (a) Outline the terms and conditions for the provision of pharmacy or pharmacist

    services;

    (b) Prohibit the insurer, pharmacy benefit manager, or other administrator from:

    1. Reducing payment for pharmacy or pharmacist services, directly or

    indirectly, under a reconciliation process to an effective rate of

    reimbursement. This prohibition shall include, without limitation,

    creating, imposing, or establishing direct or indirect remuneration fees,

    generic effective rates, dispensing effective rates, brand effecti ve rates,

    any other effective rates, in -network fees, performance fees, point -of-

    sale fees, retroactive fees, pre -adjudication fees, post -adjudication fees,

    and any other mechanism that reduces, or aggregately reduces, payment

    for pharmacy or pharmacist services;

    2. Retroactively denying, reducing reimbursement for, or seeking any

    refunds or recoupments for a claim for pharmacy or pharmacist services,

    in whole or in part, from the pharmacy or pharmacist after returning a

    paid claim response as part of the a djudication of the claim, including

    claims for the cost of a medication or dispensed product and claims for

    pharmacy or pharmacist services that are deemed ineligible for

    coverage, unless one (1) or more of the following occurred:

    a. The original claim was submitted fraudulently; or

    b. The pharmacy or pharmacist received an actual overpayment;

    3. Reimbursing the pharmacy or pharmacist for a prescription drug or other

    service at a net amount that is lower than the amount the insurer,

    pharmacy benefit manager , or other administrator reimburses itself or a

    pharmacy affiliate for the same:

    a. Prescription drug by national drug code number; or

    b. Service;

    4. Collecting cost sharing from a pharmacy or pharmacist that was

    provided to the pharmacy or pharmacist by a n insured for the provision

    of pharmacy or pharmacist services under the health plan; and

    5. Designating a prescription drug as a specialty drug unless the drug is a

    limited distribution drug that:

    a. Requires special handling; and

    b. Is not commonly carri ed at retail pharmacies or oncology clinics

    or practices; and

    (c) Notwithstanding any other law, provide the following minimum

    reimbursements to the pharmacy or pharmacist for each prescription drug or

    other service provided by the pharmacy or pharmacist:

    1. a. Except as provided in subdivision b. of this subparagraph,

    reimbursement for the cost of the drug or other service at an

    amount that is not less than:

    i. The national average drug acquisition cost for the drug or

    service at the time the drug or servi ce is administered,

    dispensed, or provided; or

    ii. If the national average drug acquisition cost is not available

    at the time a drug is administered or dispensed, the wholesale

    acquisition cost for the drug at the time the drug is

    administered or dispensed.

    b. The minimum reimbursement for the cost of a drug or other

    service required under this subparagraph shall not apply to a

    pharmacy permitted under KRS Chapter 315 with a designated

    pharmacy type of "retail chain" on file with the Kentucky Board of

    Pharmacy, or a pharmacist practicing at such a pharmacy, until a

    determination by the commissioner under subparagraph 2.a. of this

    paragraph has taken effect.

    c. For purposes of complying with this subparagraph, the insurer,

    pharmacy benefit manager, or other administrator shall utilize the

    most recently published monthly national average drug acquisition

    cost as a point of reference for the ingredient drug product

    component of a pharmacy's or pharmacist's reimbursement for

    drugs appearing on the national average drug acquisition cost list;

    and

    2. a. Except as provided in subdivision b. of this subparagraph, for

    health plan years beginning on or after January 1, 202 7,

    reimbursement for a professional dispensing fee that is not less

    than the average cost to dispense a prescription drug in an

    ambulatory pharmacy located in Kentucky, as determined by the

    commissioner in an administrative regulation promulgated in

    accordance with KRS Chapter 13A.

    b. i. The minimum dispensing fee required under subdivision a.

    of this subparagraph shall not apply to a mail -order

    pharmaceutical distributor, including a mail-order pharmacy.

    ii. For health plan years beginning prior to January 1, 2027, and

    for any future health plan years for which a determination by

    the commissioner under subdivision a. of this subparagraph

    has not taken effect, the minimum dispensing fee for a

    pharmacy permitted under KRS Chapter 315 with a

    designated pharmac y type of "retail independent" on file

    with the Kentucky Board of Pharmacy, or a pharmacist

    practicing at such a pharmacy, shall be not less than ten

    dollars and sixty-four cents ($10.64).

    c. In acquiring data for, and making, the determination required

    under subdivision a. of this subparagraph, the commissioner shall:

    i. Promulgate an administrative regulation in accordance with

    KRS Chapter 13A that establishes the data elements to be

    collected by the Kentucky Board of Pharmacy under KRS

    315.038;

    ii. Conduct a study of the dispensing data submitted to the

    commissioner by the Kentucky Board of Pharmacy in

    accordance with KRS 315.038;

    iii. Repeat the study every two (2) years to obtain updated

    information;

    iv. Adjust the determination every two (2) years as appropriate

    based upon the results of each study; and

    v. Comply with all requirements of KRS 315.038.

    d. In carrying out his or her duties under this subparagraph, the

    commissioner shall cooperate and consult with the Kentucky

    Board of Pharmacy.

    Collected 2026-09-05T20:57:47Z. Source file · JSON

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