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A05882 Summary:

BILL NOA05882B
 
SAME ASSAME AS S05939-B
 
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
 
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 Text:



 
                STATE OF NEW YORK
        ________________________________________________________________________
 
                                         5882--B
 
                               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, JONES, SIMONE, ALVAREZ, RAJKUMAR,
          REYES, BURDICK, LASHER, LUPARDO, BARRETT, RA, ROSENTHAL, SIMON,  McDO-
          NOUGH,  BENEDETTO,  ZACCARO, DeSTEFANO, BLUMENCRANZ -- 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 amendments, ordered reprinted as amended and recommit-
          ted 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:
     3    (j) "Pharmacy acquisition cost rate" means the cost paid by a  partic-
     4  ipating  pharmacy  to  acquire  generic,  brand  name drugs, or biologic
     5  products, or drugs produced through genetic technology or  biopharmaceu-
     6  tical processes pursuant to cost invoices from the pharmacy.
     7    (k)  "National average drug acquisition cost" means the monthly survey
     8  of retail pharmacies conducted by the federal Centers for  Medicare  and
     9  Medicaid  Services (CMS) to determine average acquisition cost for Medi-
    10  caid covered outpatient drugs.
    11    § 2. Subdivision 3 of section 280-a  of  the  public  health  law,  as
    12  amended  by  chapter  128  of  the  laws  of 2022, is amended to read as
    13  follows:
    14    3. Prescriptions. (a) A pharmacy benefit manager may not substitute or
    15  cause the substituting of one prescription drug for another in  dispens-
    16  ing  a  prescription,  or  alter or cause the altering of the terms of a
 
         EXPLANATION--Matter in italics (underscored) is new; matter in brackets
                              [ ] is old law to be omitted.
                                                                   LBD01972-08-5

        A. 5882--B                          2
 
     1  prescription, except with the approval of the prescriber or as explicit-
     2  ly required or permitted by law, including regulations of the department
     3  of financial services or the department of  health.  The  superintendent
     4  and  commissioner,  in  coordination  with each other, are authorized to
     5  promulgate regulations to determine when  substitution  of  prescription
     6  drugs may be required or permitted.
     7    (b)  To  the  extent  permitted  under federal law, a pharmacy benefit
     8  manager shall pay a participating pharmacy at minimum  at  the  national
     9  average  drug  acquisition cost (NADAC) rate or at the pharmacy acquisi-
    10  tion cost rate if there  is  not  a  NADAC  rate,  plus  a  professional
    11  dispensing  fee  that is at minimum the professional dispensing fee paid
    12  under the state medical assistance  program.  For  generic,  brand  name
    13  medications,  biologic products, or drugs produced through genetic tech-
    14  nology or biopharmaceutical processes as required by a  manufacturer,  a
    15  federal  or  state  regulatory  agency, or accrediting body that require
    16  unique handling, distribution or administration, in-depth patient teach-
    17  ing, coordination of care, or frequent or special monitoring  to  ensure
    18  successful  use,  special  packaging,  shipping  or  other  costs  to be
    19  incurred by the pharmacy for the dispensing process that is greater than
    20  the professional dispensing fee paid by  the  state  medical  assistance
    21  program,  participating pharmacies shall be paid a professional dispens-
    22  ing fee for these costs to ensure a participating pharmacy is  not  paid
    23  less  than  its  cost  to acquire and dispense medications.   A pharmacy
    24  benefit manager shall not pay a participating pharmacy below its pharma-
    25  cy acquisition cost but may require demonstration of such  cost  through
    26  the  provision  of  pharmacy invoices. Provided, however, this paragraph
    27  shall not apply to prescriptions, prescription drugs,  or  payments  for
    28  prescription  drugs,  distributed, or paid for in whole or in part, by a
    29  trust  fund  established  or  maintained  under  the  Labor   Management
    30  Relations Act (29 U.S. Code § 186), pursuant to coverage required by the
    31  terms  of  a  collective  bargaining agreement between an employer and a
    32  labor organization or certified employee organization; or pursuant to  a
    33  health plan, welfare fund, pharmaceutical plan, or other form of medical
    34  or  prescription  coverage  established,  adopted,  utilized, funded, or
    35  agreed upon by an employer and a labor organization or certified employ-
    36  ee organization pursuant to a collective bargaining agreement; or, where
    37  the plan, coverage, fund, or program has been collectively bargained and
    38  pertains to a sponsored multi-employer plan, including but  not  limited
    39  to,  plans  developed under article five-G of the general municipal law,
    40  articles forty-four and forty-seven of the insurance law, or  any  plans
    41  created  pursuant  to  the  Internal  Revenue  Code, Employee Retirement
    42  Income Security Act or any applicable federal statute that provides such
    43  benefits to employee and retiree groups.
    44    § 3. The opening paragraph of subdivision 4 of section  280-a  of  the
    45  public  health  law,  as  added  by  chapter 828 of the laws of 2021, is
    46  amended to read as follows:
    47    A pharmacy benefit manager shall, with respect to contracts between  a
    48  pharmacy  benefit  manager  and a pharmacy or, alternatively, a pharmacy
    49  benefit manager and a pharmacy's contracting agent, such as  a  pharmacy
    50  services  administrative  organization,  include a reasonable process to
    51  appeal, investigate and resolve disputes regarding multi-source generic,
    52  brand name, and biologic product, and  drugs  produced  through  genetic
    53  technology  or  biopharmaceutical  processes  drug  pricing. The appeals
    54  process shall include the following provisions:
    55    § 4. Section 2911 of the insurance law is  amended  by  adding  a  new
    56  subsection (d) to read as follows:

        A. 5882--B                          3
 
     1    (d)  To  the  extent  permitted  under federal law, a pharmacy benefit
     2  manager shall pay a participating pharmacy at minimum  at  the  national
     3  average  drug  acquisition  cost (NADAC) rate, as defined in subdivision
     4  one of section two hundred eighty-a of the public health law, or at  the
     5  pharmacy acquisition cost rate, as defined in subdivision one of section
     6  two  hundred  eighty-a of the public health law, if there is not a NADAC
     7  rate, plus a professional dispensing fee that is at minimum the  profes-
     8  sional  dispensing  fee paid under the state medical assistance program.
     9  For  generic,  brand  name  medications,  biologic  products,  or  drugs
    10  produced  through  genetic  technology or biopharmaceutical processes as
    11  required by a manufacturer, a federal or  state  regulatory  agency,  or
    12  accrediting  body that require unique handling, distribution or adminis-
    13  tration, in-depth patient teaching, coordination of care, or frequent or
    14  special monitoring to ensure successful use, special packaging, shipping
    15  or other costs to be incurred by the pharmacy for the dispensing process
    16  that is greater than the professional dispensing fee paid by  the  state
    17  medical  assistance  program,  participating  pharmacies shall be paid a
    18  professional dispensing fee for these costs to  ensure  a  participating
    19  pharmacy  is not paid less than its cost to acquire and dispense medica-
    20  tions. A pharmacy benefit manager shall not pay a participating pharmacy
    21  below its pharmacy acquisition cost but  may  require  demonstration  of
    22  such cost through the provision of pharmacy invoices. A pharmacy benefit
    23  manager  shall,  with  respect  to  contracts between a pharmacy benefit
    24  manager and a pharmacy or, alternatively, a pharmacy benefit manager and
    25  a pharmacy's contracting agent, such as a pharmacy services  administra-
    26  tive  organization,  include a reasonable process to appeal, investigate
    27  and resolve disputes regarding multi-source generic, brand name, biolog-
    28  ic product, and drugs produced through genetic technology or  biopharma-
    29  ceutical processes drug pricing. The appeals process shall be considered
    30  within  the  existing appeals process under section two hundred eighty-a
    31  of the public health law.  Provided, however, this paragraph  shall  not
    32  apply to prescriptions, prescription drugs, or payments for prescription
    33  drugs,  distributed,  or  paid  for in whole or in part, by a trust fund
    34  established or maintained under the Labor Management Relations  Act  (29
    35  U.S.  Code  §  186),  pursuant  to  coverage  required by the terms of a
    36  collective bargaining agreement between an employer and a  labor  organ-
    37  ization  or  certified  employee  organization;  or pursuant to a health
    38  plan, welfare fund, pharmaceutical plan, or other  form  of  medical  or
    39  prescription  coverage established, adopted, utilized, funded, or agreed
    40  upon by an employer and  a  labor  organization  or  certified  employee
    41  organization  pursuant  to  a collective bargaining agreement; or, where
    42  the plan, coverage, fund, or program has been collectively bargained and
    43  pertains to a sponsored multi-employer plan, including but  not  limited
    44  to,  plans  developed under article five-G of the general municipal law,
    45  articles forty-four and forty-seven of the insurance law, or  any  plans
    46  created  pursuant  to  the  Internal  Revenue  Code, Employee Retirement
    47  Income Security Act or any applicable federal statute that provides such
    48  benefits to employee and retiree groups.
    49    § 5. This act shall take effect January 1, 2026 and shall apply to all
    50  policies and contracts issued, renewed, modified, altered or amended  on
    51  and after such date.
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