Bill Text: NY A04667 | 2021-2022 | General Assembly | Introduced
Bill Title: Provides for patient access to FDA approved abuse-deterrent technology to help combat opioid abuse.
Spectrum: Partisan Bill (Democrat 1-0)
Status: (Introduced - Dead) 2022-01-05 - referred to insurance [A04667 Detail]
Download: New_York-2021-A04667-Introduced.html
STATE OF NEW YORK ________________________________________________________________________ 4667 2021-2022 Regular Sessions IN ASSEMBLY February 4, 2021 ___________ Introduced by M. of A. SAYEGH -- read once and referred to the Committee on Insurance AN ACT to amend the public health law and the insurance law, in relation to the use of abuse-deterrent technology for opioids as a mechanism for reducing abuse and diversion of opioid drugs The People of the State of New York, represented in Senate and Assem- bly, do enact as follows: 1 Section 1. Section 273 of the public health law is amended by adding a 2 new subdivision 11 to read as follows: 3 11. Any prior authorization requirements for opioid analgesic and any 4 service denials made pursuant thereto shall not require use of opioid 5 analgesic drug products without abuse-deterrent properties before 6 authorizing the use of abuse-deterrent opioid analgesic drug products. 7 § 2. The insurance law is amended by adding a new section 3216-a to 8 read as follows: 9 § 3216-a. Access to abuse-deterrent opioid medications. (a) An insur- 10 ance carrier or health plan shall provide coverage on its formulary, 11 drug list or other lists of similar construct for at least one abuse- 12 deterrent opioid analgesics drug product per opioid analgesics active 13 ingredient. 14 (1) Cost-sharing for brand name abuse-deterrent opioid analgesic drug 15 products covered pursuant to this section shall not exceed the lowest 16 cost-sharing level applied to brand name non-abuse deterrent opioid 17 drugs covered under the applicable health plan or policy. 18 (2) Cost-sharing for generic abuse-deterrent opioid analgesic drug 19 products covered pursuant to this section shall not exceed the lowest 20 cost-sharing level applied to generic non-abuse deterrent opioid drugs 21 covered under the applicable health plan or policy. 22 (3) An increase in patient cost-sharing or disincentives for prescri- 23 bers or dispensers shall not be allowed to achieve compliance with this 24 section. EXPLANATION--Matter in italics (underscored) is new; matter in brackets [] is old law to be omitted. LBD06823-01-1A. 4667 2 1 (b) Any prior-authorization requirements or other utilization review 2 measures for opioid analgesics, and any service denials made pursuant 3 thereto, shall not require use of opioid analgesic drug products without 4 abuse-deterrent properties in order to access abuse-deterrent opioid 5 analgesic drug products. 6 (c) Definitions. As used in this section: 7 (1) "Opioid analgesic drug product" means a drug in the opioid anal- 8 gesic drug class prescribed to treat moderate to severe pain or other 9 conditions, whether in immediate release or extended long acting release 10 form and whether or not combined with other drug substances to form a 11 single drug product or other dosage form. 12 (2) "Abuse deterrent opioid analgesic drug product" means a brand or 13 generic opioid analgesic drug product approved by the federal food and 14 drug administration with abuse-deterrence labeling claims indicating its 15 abuse-deterrent properties are expected to deter or reduce its abuse. 16 (3) "Cost-sharing" means any coverage limit, copayment, coinsurance, 17 deductible or other out-of-pocket patient expense requirements. 18 § 3. This act shall take effect on the one hundred twentieth day after 19 it shall have become a law, and shall apply to all policies and 20 contracts issued, renewed, modified, altered or amended on or after such 21 date.