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A05882 Summary:

BILL NOA05882C
 
SAME ASSAME AS S05939-C
 
SPONSORMcDonald
 
COSPNSRWoerner, Bologna, Dais, Griffin, Hevesi, Stirpe, Lee, Kay, Brabenec, Buttenschon, Shimsky, Glick, McMahon, Manktelow, Angelino, Brown K, Blankenbush, Romero, Otis, Paulin, Dinowitz, Solages, Sayegh, Gallahan, Jones, Simone, Alvarez, Rajkumar, Reyes, Burdick, Lasher, Lupardo, Barrett, Ra, Rosenthal, Simon, McDonough, Benedetto, Zaccaro, DeStefano, Blumencranz, Miller, Sempolinski, Chludzinski, Palmesano, Lemondes, Beephan, Maher, Lavine, Weprin, Pheffer Amato, Simpson, Hunter, Fitzpatrick, Burroughs, Novakhov, Slater, Stern, Steck, Bailey, De Los Santos, Clark, Shrestha, Wieder, Magnarelli, Seawright, Conrad, Jacobson, Eachus, Gray, Cruz, Williams, Schiavoni, Bendett, Jensen, Lunsford, Kelles, Bronson, Tapia, Davila, Meeks, Gonzalez-Rojas, Bores, Rivera, Mikulin, Santabarbara, Kassay, Hyndman, Gallagher, Rozic, Braunstein, Burke, Carroll P, Lucas, Peoples-Stokes, Yeger, Taylor, Forrest, Anderson, Bichotte Hermelyn, Carroll R, Chandler-Waterman, Colton, Cook, Cunningham, Dilan, Fall, Gibbs, Giglio, Hawley, Hooks, Jackson, Kim, Morinello, O'Pharrow, Ramos, Septimo, Walker, Wright, Zinerman
 
MLTSPNSRLevenberg
 
Amd §280-a, Pub Health L; amd §2911, Ins L
 
Requires a pharmacy benefit manager to pay a participating pharmacy at minimum at the national average drug acquisition cost (NADAC) rate, or at the pharmacy acquisition cost rate if greater or there is not a NADAC rate, plus a professional dispensing fee that is at minimum the professional dispensing fee paid under the state medical assistance program.
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A05882 Actions:

BILL NOA05882C
 
02/24/2025referred to health
06/09/2025amend and recommit to health
06/09/2025print number 5882a
06/09/2025amend and recommit to health
06/09/2025print number 5882b
07/02/2025reference changed to insurance
01/07/2026referred to insurance
02/24/2026amend and recommit to insurance
02/24/2026print number 5882c
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A05882 Memo:

NEW YORK STATE ASSEMBLY
MEMORANDUM IN SUPPORT OF LEGISLATION
submitted in accordance with Assembly Rule III, Sec 1(f)
 
BILL NUMBER: A5882C
 
SPONSOR: McDonald
  TITLE OF BILL: An act to amend the public health law and the insurance law, in relation to payments by pharmacy benefit managers to participating pharmacies   PURPOSE OF THE BILL: The Patient Access to Pharmacy Act (PAPA) seeks to simplify and change the methodology for pharmacy reimbursement for commercial health plans to a Cost-Plus model that is more transparent for patients, payors, and pharmacies while saving costs through the process.   SUMMARY OF SPECIFIC PROVISIONS: Section 1: Amends subdivision 1 of section 280-a of the public health law by adding paragraphs (j) and (k). To define the Pharmacy Acquisition Cost Rate as the cost a participating pharmacy pays to acquire drugs, including generic, brand-name, biologics, and those produced through genetic or biopharmaceutical processes, based on pharmacy cost invoices. It also defines the National Average Drug Acquisition Cost as the month- ly survey conducted by the Centers for Medicare and Medicaid Services (CMS) to determine the average acquisition cost of Medicaid-covered outpatient drugs. Section 2: Amends subdivision 3 of section 280-a of the public health law to add a paragraph (b). To prohibit pharmacy benefit managers from substituting or altering prescription drugs without prescriber approval or legal authorization. The superintendent and commissioner may issue regulations on when substitutions are permitted. Additionally, pharmacy benefit managers must reimburse participating pharmacies at least the National Average Drug Acquisition Cost (NADAC) rate or the Pharmacy Acquisition Cost Rate, whichever is higher, plus a professional dispens- ing fee equal to that paid under the state medical assistance program. For medications requiring specialized handling, distribution, adminis- tration, patient education, care coordination, monitoring, special pack- aging, or shipping, pharmacies must receive an additional dispensing fee to ensure they are not reimbursed below their acquisition and dispensing costs. Section 3: Amends the opening paragraph of subdivision 4 of section 280-a of the public health law. To require pharmacy benefit managers to establish a reasonable process for pharmacies or their contracting agents to appeal, investigate, and resolve disputes over drug pricing for multi-source generics, brand-name drugs, biologics, and drugs produced through genetic or biopharmaceutical processes. Section 4: Amends section 2911 of the insurance law to add a new subsection (d) to ensure that pharmacy benefit managers reimburse phar- macies fairly by covering the actual cost of acquiring and dispensing medications. It mandates payment at either the National Average Drug Acquisition Cost (NADAC) rate or the Pharmacy Acquisition Cost Rate, if there is not a NADAC rate, along with a professional dispensing fee. Additional compensation is required for drugs needing special handling, administration, or monitoring. The amendment also establishes a stand- ardized appeals process for pharmacies to dispute pricing issues. This paragraph does not apply to prescriptions or prescription drugs that are distributed or paid for by a trust fund established under the Labor Management Relations Act, or provided through a health, welfare, or pharmaceutical plan that has been created, adopted, or funded as part of a collective bargaining agreement between an employer and a labor organ- ization or certified employee organization. Section 5: Sets Effective Date.   JUSTIFICATION: The Patient Access to Pharmacy Act (PAPA) is part of a continued to effort to lower prescription drug costs for patients, stabilize and potentially improve pharmacy access in underserved areas, and provide greater transparency on what plan sponsors/employers are paying for prescription drug costs which will lead to cost savings. This is the same reimbursement methodology adopted by New York State Medicaid in 2023 which has led to consistent patient coverage and enhanced rebate revenues which has' stabilized the cost of, the prescription program. The methodology is known as Cost-Plus. Pharmacy Benefit Managers (PBMs) serve an important part of delivering pharmacy services as they work on behalf of the plan sponsors or employers to manage the pharmacy benefit. Historically their purpose is to process claims; however, over the past 20 years they have negotiated in an opaque environment with the pharma- ceutical companies for rebates which are alleged to lower the cost of prescription benefits. However, the cost-savings is not realized with patients or those paying for the pharmacy benefit cost. Year over year insurance premiums for commercial health plans rise between 8-13% of which pharmaceutical companies being blamed as the main culprit..This is despite the fact that in 2024, average brand-name drugs' list prices grew by only 2.3%. After adjusting for overall inflation, brand-name drug net prices dropped for an unprecedented seventh consecutive year according to industry analysts. This is due to the rebate pumping phenomenon where the PBMs solicit a rebate from the manufacturer, the manufacturer raises the price and the PBM solicits a greater rebate creating the gross-tonet bubbled In light of the fact that PBMs are licensed and monitored by the New York State Department of Financial Services (DFS), it is time to continue to shine light on the true cost of drug costs by using a national standard for determining cost benchmarks for pharmacy reimbursement by using the National Average Drug Acquisition Cost (NADAC) which is a national monthly survey of actual costs incurred by pharmacies to acquire medications. The Cost-Plus methodology moves away from the prior Average Wholesale Price (AWP) - reimbursement which was grossly overinflated as well as the Wholesaler Acquisition Cost (WAC) and Maximum Acquisition Cost (MAC) pricing methodology which were not consistent and did not provide an actual picture of pharmaceutical costs. NADAC is a nationally accepted benchmark, so recognized that the three major PBMs that control over 80% of all pharmacy claims have announced that they are moving to the Cost- Plus model for commercial plans in 2026. The PAPA is also important considering the years of findings established in a bi-partisan manner by the US Congress and the Federal Trade Commis- sion (FTC) which have found that PBMs have established reimbursement methodologies that reimburse their own pharmacies more than traditional independent pharmacies or direct high-cost specialty business to their own operations. Although the big 3 PBMs deny this accusation, the FTC has been highly critical of their activities and the current 119th Congress is pursuing methods to provide greater scrutiny, transparency, and stewardship of public dollars. Passage of the PAPA will provide a very clear guide for reimbursement of pharmaceuticals which will benefit both the patient and the payor while providing stable reimbursement to pharmacies regardless of their owner or location.   LEGISLATIVE HISTORY: 2023-2024: A.10327/S.9570   FISCAL IMPLICATIONS: None to the state   EFFECTIVE DATE: This act shall take effect January 1, 2026 and apply to all policies and contracts issued, renewed, modified, altered or amended on and after such date.
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A05882 Text:



 
                STATE OF NEW YORK
        ________________________________________________________________________
 
                                         5882--C
 
                               2025-2026 Regular Sessions
 
                   IN ASSEMBLY
 
                                    February 24, 2025
                                       ___________
 
        Introduced  by M. of A. McDONALD, WOERNER, BOLOGNA, DAIS, GRIFFIN, HEVE-
          SI, STIRPE, LEE, KAY, BRABENEC, BUTTENSCHON, SHIMSKY, GLICK,  McMAHON,
          MANKTELOW,  ANGELINO,  K. BROWN,  BLANKENBUSH,  ROMERO,  OTIS, PAULIN,
          DINOWITZ, SOLAGES, SAYEGH, GALLAHAN, SIMONE, ALVAREZ, RAJKUMAR, REYES,
          BURDICK, LASHER, LUPARDO, BARRETT, RA,  ROSENTHAL,  SIMON,  McDONOUGH,
          BENEDETTO,   ZACCARO,  DeSTEFANO,  BLUMENCRANZ,  MILLER,  SEMPOLINSKI,
          CHLUDZINSKI, PALMESANO,  LEMONDES,  BEEPHAN,  MAHER,  LAVINE,  WEPRIN,
          PHEFFER AMATO,  SIMPSON,  HUNTER,  FITZPATRICK,  BURROUGHS,  NOVAKHOV,
          SLATER, STERN, STECK, BAILEY, DE LOS SANTOS, CLARK, SHRESTHA,  WIEDER,
          MAGNARELLI, SEAWRIGHT, CONRAD, JACOBSON, EACHUS, GRAY, CRUZ, WILLIAMS,
          SCHIAVONI,  BENDETT, JENSEN, LUNSFORD, KELLES, BRONSON, TAPIA, DAVILA,
          MEEKS, GONZALEZ-ROJAS, BORES, RIVERA, MIKULIN,  SANTABARBARA,  KASSAY,
          HYNDMAN,  GALLAGHER,  ROZIC,  BRAUNSTEIN,  BURKE,  P. CARROLL,  LUCAS,
          PEOPLES-STOKES, YEGER, TAYLOR, FORREST, R. CARROLL, CUNNINGHAM, DILAN,
          FALL, HAWLEY, HOOKS,  JACKSON,  KIM,  MORINELLO,  O'PHARROW,  SEPTIMO,
          WALKER,  WRIGHT,  ZINERMAN -- Multi-Sponsored by -- M. of A. LEVENBERG
          -- read once and referred to the  Committee  on  Health  --  committee
          discharged, bill amended, ordered reprinted as amended and recommitted
          to  said  committee  -- again reported from said committee with amend-
          ments, ordered reprinted as amended and recommitted to said  committee
          --  reference  changed to the Committee on Insurance -- recommitted to
          the Committee on Insurance in accordance with Assembly Rule 3, sec.  2
          --  committee  discharged,  bill amended, ordered reprinted as amended
          and recommitted to said committee
 
        AN ACT to amend the public health law and the insurance law, in relation
          to payments by pharmacy benefit managers to participating pharmacies
 
          The People of the State of New York, represented in Senate and  Assem-
        bly, do enact as follows:
 
     1    Section  1. Subdivision 1 of section 280-a of the public health law is
     2  amended by adding two new paragraphs (j) and (k) to read as follows:

         EXPLANATION--Matter in italics (underscored) is new; matter in brackets
                              [ ] is old law to be omitted.
                                                                   LBD01972-10-6

        A. 5882--C                          2
 
     1    (j) "Pharmacy acquisition cost rate" means the cost paid by a  partic-
     2  ipating  pharmacy  to  acquire  generic,  brand  name drugs, or biologic
     3  products, or drugs produced through genetic technology or  biopharmaceu-
     4  tical processes pursuant to cost invoices from the pharmacy.
     5    (k)  "National average drug acquisition cost" means the monthly survey
     6  of retail pharmacies conducted by the federal Centers for  Medicare  and
     7  Medicaid  Services (CMS) to determine average acquisition cost for Medi-
     8  caid covered outpatient drugs.
     9    § 2. Subdivision 3 of section 280-a  of  the  public  health  law,  as
    10  amended  by  chapter  128  of  the  laws  of 2022, is amended to read as
    11  follows:
    12    3. Prescriptions. (a) A pharmacy benefit manager may not substitute or
    13  cause the substituting of one prescription drug for another in  dispens-
    14  ing  a  prescription,  or  alter or cause the altering of the terms of a
    15  prescription, except with the approval of the prescriber or as explicit-
    16  ly required or permitted by law, including regulations of the department
    17  of financial services or the department of  health.  The  superintendent
    18  and  commissioner,  in  coordination  with each other, are authorized to
    19  promulgate regulations to determine when  substitution  of  prescription
    20  drugs may be required or permitted.
    21    (b)  To  the  extent  permitted  under federal law, a pharmacy benefit
    22  manager shall pay a participating pharmacy at minimum  at  the  national
    23  average  drug  acquisition cost (NADAC) rate or at the pharmacy acquisi-
    24  tion cost rate if there  is  not  a  NADAC  rate,  plus  a  professional
    25  dispensing  fee  that is at minimum the professional dispensing fee paid
    26  under the state medical assistance  program.  For  generic,  brand  name
    27  medications,  biologic products, or drugs produced through genetic tech-
    28  nology or biopharmaceutical processes as required by a  manufacturer,  a
    29  federal  or  state  regulatory  agency, or accrediting body that require
    30  unique handling, distribution or administration, in-depth patient teach-
    31  ing, coordination of care, or frequent or special monitoring  to  ensure
    32  successful  use,  special  packaging,  shipping  or  other  costs  to be
    33  incurred by the pharmacy for the dispensing process that is greater than
    34  the professional dispensing fee paid by  the  state  medical  assistance
    35  program,  participating pharmacies shall be paid a professional dispens-
    36  ing fee for these costs to ensure a participating pharmacy is  not  paid
    37  less  than  its  cost  to acquire and dispense medications.   A pharmacy
    38  benefit manager shall not pay a participating pharmacy below its pharma-
    39  cy acquisition cost but may require demonstration of such  cost  through
    40  the  provision  of  pharmacy invoices. Provided, however, this paragraph
    41  shall not apply to prescriptions, prescription drugs,  or  payments  for
    42  prescription  drugs,  distributed, or paid for in whole or in part, by a
    43  trust  fund  established  or  maintained  under  the  Labor   Management
    44  Relations Act (29 U.S. Code § 186), pursuant to coverage required by the
    45  terms  of  a  collective  bargaining agreement between an employer and a
    46  labor organization or certified employee organization; or pursuant to  a
    47  health plan, welfare fund, pharmaceutical plan, or other form of medical
    48  or  prescription  coverage  established,  adopted,  utilized, funded, or
    49  agreed upon by an employer and a labor organization or certified employ-
    50  ee organization pursuant to a collective bargaining agreement; or, where
    51  the plan, coverage, fund, or program has been collectively bargained and
    52  pertains to a sponsored multi-employer plan, including but  not  limited
    53  to,  plans  developed under article five-G of the general municipal law,
    54  articles forty-four and forty-seven of the insurance law, or  any  plans
    55  created  pursuant  to  the  Internal  Revenue  Code, Employee Retirement

        A. 5882--C                          3
 
     1  Income Security Act or any applicable federal statute that provides such
     2  benefits to employee and retiree groups.
     3    §  3.  The  opening paragraph of subdivision 4 of section 280-a of the
     4  public health law, as added by chapter 828  of  the  laws  of  2021,  is
     5  amended to read as follows:
     6    A  pharmacy benefit manager shall, with respect to contracts between a
     7  pharmacy benefit manager and a pharmacy or,  alternatively,  a  pharmacy
     8  benefit  manager  and a pharmacy's contracting agent, such as a pharmacy
     9  services administrative organization, include a  reasonable  process  to
    10  appeal, investigate and resolve disputes regarding multi-source generic,
    11  brand  name,  and  biologic  product, and drugs produced through genetic
    12  technology or biopharmaceutical  processes  drug  pricing.  The  appeals
    13  process shall include the following provisions:
    14    §  4.  Section  2911  of  the insurance law is amended by adding a new
    15  subsection (d) to read as follows:
    16    (d) To the extent permitted under  federal  law,  a  pharmacy  benefit
    17  manager  shall  pay  a participating pharmacy at minimum at the national
    18  average drug acquisition cost (NADAC) rate, as  defined  in  subdivision
    19  one  of section two hundred eighty-a of the public health law, or at the
    20  pharmacy acquisition cost rate, as defined in subdivision one of section
    21  two hundred eighty-a of the public health law, if there is not  a  NADAC
    22  rate,  plus a professional dispensing fee that is at minimum the profes-
    23  sional dispensing fee paid under the state medical  assistance  program.
    24  For  generic,  brand  name  medications,  biologic  products,  or  drugs
    25  produced through genetic technology or  biopharmaceutical  processes  as
    26  required  by  a  manufacturer,  a federal or state regulatory agency, or
    27  accrediting body that require unique handling, distribution or  adminis-
    28  tration, in-depth patient teaching, coordination of care, or frequent or
    29  special monitoring to ensure successful use, special packaging, shipping
    30  or other costs to be incurred by the pharmacy for the dispensing process
    31  that  is  greater than the professional dispensing fee paid by the state
    32  medical assistance program, participating pharmacies  shall  be  paid  a
    33  professional  dispensing  fee  for these costs to ensure a participating
    34  pharmacy is not paid less than its cost to acquire and dispense  medica-
    35  tions. A pharmacy benefit manager shall not pay a participating pharmacy
    36  below  its  pharmacy  acquisition  cost but may require demonstration of
    37  such cost through the provision of pharmacy invoices. A pharmacy benefit
    38  manager shall, with respect to  contracts  between  a  pharmacy  benefit
    39  manager and a pharmacy or, alternatively, a pharmacy benefit manager and
    40  a  pharmacy's contracting agent, such as a pharmacy services administra-
    41  tive organization, include a reasonable process to  appeal,  investigate
    42  and resolve disputes regarding multi-source generic, brand name, biolog-
    43  ic  product, and drugs produced through genetic technology or biopharma-
    44  ceutical processes drug pricing. The appeals process shall be considered
    45  within the existing appeals process under section two  hundred  eighty-a
    46  of  the  public health law.  Provided, however, this paragraph shall not
    47  apply to prescriptions, prescription drugs, or payments for prescription
    48  drugs, distributed, or paid for in whole or in part,  by  a  trust  fund
    49  established  or  maintained under the Labor Management Relations Act (29
    50  U.S. Code § 186), pursuant to  coverage  required  by  the  terms  of  a
    51  collective  bargaining  agreement between an employer and a labor organ-
    52  ization or certified employee organization;  or  pursuant  to  a  health
    53  plan,  welfare  fund,  pharmaceutical  plan, or other form of medical or
    54  prescription coverage established, adopted, utilized, funded, or  agreed
    55  upon  by  an  employer  and  a  labor organization or certified employee
    56  organization pursuant to a collective bargaining  agreement;  or,  where

        A. 5882--C                          4

     1  the plan, coverage, fund, or program has been collectively bargained and
     2  pertains  to  a sponsored multi-employer plan, including but not limited
     3  to, plans developed under article five-G of the general  municipal  law,
     4  articles  forty-four  and  forty-seven  of  this  chapter,  or any plans
     5  created pursuant to  the  Internal  Revenue  Code,  Employee  Retirement
     6  Income Security Act or any applicable federal statute that provides such
     7  benefits to employee and retiree groups.
     8    § 5. This act shall take effect January 1, 2027 and shall apply to all
     9  policies  and contracts issued, renewed, modified, altered or amended on
    10  and after such date.
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