Bill Text: NH HB1697 | 2020 | Regular Session | Introduced
Bill Title: Relative to prescription drug discount prohibition.
Spectrum: Partisan Bill (Democrat 1-0)
Status: (Introduced - Dead) 2020-08-19 - Full Committee Work Session: 09/01/2020 02:00 pm Members of the public may attend using this link: https://www.zoom.us/j/99708430633 - Executive Session to Follow [HB1697 Detail]
Download: New_Hampshire-2020-HB1697-Introduced.html
HB 1697-FN - AS INTRODUCED
2020 SESSION
20-3097
01/05
HOUSE BILL 1697-FN
AN ACT relative to prescription drug discount prohibition.
SPONSORS: Rep. Butler, Carr. 7; Rep. Muscatel, Graf. 12
COMMITTEE: Commerce and Consumer Affairs
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ANALYSIS
This bill prohibits, with limited exceptions, prescription drug manufacturers from offering coupons or discounts to cover insurance copayments or deductibles.
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Explanation: Matter added to current law appears in bold italics.
Matter removed from current law appears [in brackets and struckthrough.]
Matter which is either (a) all new or (b) repealed and reenacted appears in regular type.
20-3097
01/05
STATE OF NEW HAMPSHIRE
In the Year of Our Lord Two Thousand Twenty
AN ACT relative to prescription drug discount prohibition.
Be it Enacted by the Senate and House of Representatives in General Court convened:
1 New Subdivision; Prescription Drug Discount Prohibition. Amend RSA 318 by inserting after section 66 the following new subdivision:
Prescription Drug Discount Prohibition
318:67 Prescription Drug Discount Prohibition; Exceptions.
I.(a) Except as provided in paragraph III, a pharmacy shall not accept as payment from a patient on behalf of a person who manufactures a prescription drug, a discount, repayment, product voucher, or other reduction in an individual's out-of-pocket expenses associated with his or her health insurance, health care service plan, or other health coverage, including but not limited to, a copayment, coinsurance, or deductible for a prescription drug if a lower cost form of that drug is covered under the individual's health insurance, health care service plan, or other health coverage on a lower cost-sharing tier that is designated to be therapeutically equivalent as indicated by the United States Food and Drug Administration's (FDA) "Approved Drug Products with Therapeutic Equivalence Evaluations."
(b) The prohibition in subparagraph (a) shall not apply to a branded prescription drug, until the time that the first drug designated in the FDA's "Approved Drug Products with Therapeutic Equivalence Evaluations" as therapeutically equivalent to that branded prescription drug has been nationally available for 6 calendar months.
(c) A coupon may be accepted as payment if the individual’s out-of-pocket expenses associated with the lower cost form of the drug exceeds $500.
II. Except as provided in paragraph IV, a pharmacy shall not accept as payment from a patient on behalf of a person who manufactures a prescription drug, a discount, repayment, product voucher, or other reduction in the individual's out-of-pocket expenses associated with his or her health insurance, health care service plan, or other health coverage, including but not limited to a copayment, coinsurance, or deductible, for a prescription drug if the active ingredients of the drug are contained in products regulated by the FDA, are available without prescription at a lower cost, and are not otherwise contraindicated for treatment of the condition for which the prescription drug is approved.
III. The prohibitions in paragraphs I and II shall not apply to any of the following:
(a) A discount, repayment, product voucher, or other payment to a patient or another person on the patient's behalf for a prescription drug required under a FDA Risk Evaluation and Mitigation Strategy for the purpose of monitoring or facilitating the use of that prescription drug in a manner consistent with the approved labeling of the prescription drug.
(b) A single-tablet drug regimen for treatment or prevention of human immunodeficiency virus (HIV) or acquired immune deficiency syndrome (AIDS) that is as effective as a multitablet regimen, unless, consistent with clinical guidelines and peer-reviewed scientific and medical literature, the multitablet regimen is clinically equally effective or more effective and is more likely to result in adherence to the drug regimen.
(c) The individual patient has completed any applicable step therapy or prior authorization requirements for the branded prescription drug as mandated by the individual's present or past health insurer, health care service plan, or other health coverage.
(d) A discount, repayment, product voucher, or other reduction in an individual patient's out-of-pocket expenses for self-pay patients.
IV.(a) This subdivision shall not prohibit a pharmacy from accepting from a patient on behalf of an entity, including an entity that manufactures prescription drugs or a patient assistance program that is solely funded by one or more manufacturers, a pharmaceutical product free of any cost, if the product is free of cost to both the patient and his or her health insurer, health care service plan, or other health coverage.
(b)(1) This subdivision shall not prohibit or limit assistance to a patient provided by an independent charity patient assistance program.
(2) For purposes of this section, "independent charity patient assistance program" means a program that meets all of the following requirements:
(A) The program does not allow a pharmaceutical manufacturer or an affiliate of the manufacturer, including, but not limited to, an employee, agent, officer, shareholder, contractor, wholesaler, distributor, or pharmacy benefits manager, to exert any direct or indirect influence or control over the charity or subsidy program.
(B) Assistance is awarded in a truly independent manner that severs any link between a pharmaceutical manufacturer's funding and the beneficiary.
(C) Assistance is awarded without regard to the pharmaceutical manufacturer's interest and without regard to the beneficiary's choice of product, provider, practitioner, supplier, health insurance, health care service plan, or other health coverage.
(D) Assistance is awarded based upon a reasonable, verifiable, and uniform measure of financial need that is applied in a consistent manner.
2 New Paragraph; Managed Care Law; Provider Contract Standards. Amend RSA 420-J:8 by inserting after paragraph XV the following new paragraph:
XVI.(a)(1) Except as provided in subparagraph (c), no contract between a health carrier or pharmacy benefit manager and a participating pharmacy shall permit the pharmacy to accept as payment anything from a member on behalf of a person who manufactures a prescription drug, a discount, repayment, product voucher, or other reduction in an individual's out-of-pocket expenses associated with his or her health insurance, health care service plan, or other health coverage, including, but not limited to, a copayment, coinsurance, or deductible for a prescription drug if a lower cost form of that drug is covered under the individual's health insurance, health care service plan, or other health coverage on a lower cost-sharing tier that is designated to be therapeutically equivalent as indicated by the United States Food and Drug Administration's (FDA) "Approved Drug Products with Therapeutic Equivalence Evaluations."
(2) This prohibition shall not apply to a branded prescription drug, until the time that the first drug designated in the FDA's "Approved Drug Products with Therapeutic Equivalence Evaluations" as therapeutically equivalent to that branded prescription drug has been nationally available for 6 calendar months.
(3) Contracts may allow coupons to be accepted as payment if the individual’s out-of-pocket expenses associated with the lower cost form of the drug exceeds $500.
(b) Except as provided in subparagraph (d), no contract between a health carrier or a pharmacy benefit manager and a participating pharmacy shall permit the pharmacy to accept as payment, anything from a member on behalf of a person who manufactures a prescription drug a discount, repayment, product voucher, or other reduction in the individual's out-of-pocket expenses associated with his or her health insurance, health care service plan, or other health coverage, including, but not limited to, a copayment, coinsurance, or deductible for a prescription drug if the active ingredients of the drug are contained in products regulated by the FDA, are available without prescription at a lower cost, and are not otherwise contraindicated for treatment of the condition for which the prescription drug is approved.
(c) The prohibitions in subparagraphs (a) and (b) shall not apply to any of the following:
(1) A discount, repayment, product voucher, or other payment to a patient or another person on the patient's behalf for a prescription drug required under a FDA Risk Evaluation and Mitigation Strategy for the purpose of monitoring or facilitating the use of that prescription drug in a manner consistent with the approved labeling of the prescription drug.
(2) A single-tablet drug regimen for treatment or prevention of human immunodeficiency virus (HIV) or acquired immune deficiency syndrome (AIDS) that is as effective as a multitablet regimen, unless, consistent with clinical guidelines and peer-reviewed scientific and medical literature, the multitablet regimen is clinically equally effective or more effective and is more likely to result in adherence to the drug regimen.
(3) The individual member has completed any applicable step therapy or prior authorization requirements for the branded prescription drug as mandated by the individual's present or past health insurer, health care service plan, or other health coverage.
(4) A discount, repayment, product voucher, or other reduction in an individual patient’s out-of-pocket expenses for self-pay patients.
(d)(1) This paragraph shall not prohibit a pharmacy from accepting from a member on behalf of an entity, including an entity that manufactures prescription drugs or a patient assistance program that is solely funded by one or more manufacturers, a pharmaceutical product free of any cost, if the product is free of cost to both the member and his or her health insurer, health care service plan, or other health coverage.
(2)(A) This paragraph shall not prohibit or limit assistance to a member provided by an independent charity patient assistance program.
(B) For purposes of this subparagraph, "independent charity member assistance program" means a program that meets all of the following requirements:
(i) The program does not allow a pharmaceutical manufacturer or an affiliate of the manufacturer, including, but not limited to, an employee, agent, officer, shareholder, contractor, wholesaler, distributor, or pharmacy benefits manager, to exert any direct or indirect influence or control over the charity or subsidy program.
(ii) Assistance is awarded in a truly independent manner that severs any link between a pharmaceutical manufacturer's funding and the beneficiary.
(iii) Assistance is awarded without regard to the pharmaceutical manufacturer's interest and without regard to the beneficiary's choice of product, provider, practitioner, supplier, health insurance, health care service plan, or other health coverage.
(iv) Assistance is awarded based upon a reasonable, verifiable, and uniform measure of financial need that is applied in a consistent manner.
3 Effective Date. This act shall take effect January 1, 2021.
20-3097
12/17/19
HB 1697-FN- FISCAL NOTE
AS INTRODUCED
AN ACT relative to prescription drug discount prohibition.
FISCAL IMPACT:
Due to time constraints, the Office of Legislative Budget Assistant is unable to provide a fiscal note for this bill, as introduced, at this time. When completed, the fiscal note will be forwarded to the House Clerk's Office.
