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S05939 Summary:

BILL NOS05939C
 
SAME ASSAME AS A05882-C
 
SPONSORSKOUFIS
 
COSPNSRADDABBO, BYNOE, COONEY, FAHY, FERNANDEZ, GALLIVAN, GRIFFO, HINCHEY, JACKSON, LIU, MARTINS, MAYER, RHOADS, RIVERA, RYAN C, SALAZAR, SCARCELLA-SPANTON, STAVISKY
 
MLTSPNSR
 
Amd §280-a, Pub Health; 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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S05939 Text:



 
                STATE OF NEW YORK
        ________________________________________________________________________
 
                                         5939--C
            Cal. No. 305
 
                               2025-2026 Regular Sessions
 
                    IN SENATE
 
                                      March 4, 2025
                                       ___________
 
        Introduced  by  Sens.  SKOUFIS, ADDABBO, BYNOE, COONEY, FAHY, FERNANDEZ,
          GALLIVAN, GRIFFO,  HINCHEY,  JACKSON,  LIU,  MARTINS,  MAYER,  RHOADS,
          RIVERA,  C. RYAN,  SALAZAR,  SCARCELLA-SPANTON, STAVISKY -- read twice
          and ordered printed, and when printed to be committed to the Committee
          on Health -- committee discharged, bill amended, ordered reprinted  as
          amended  and  recommitted  to  said committee -- committee discharged,
          bill amended, ordered reprinted as amended  and  recommitted  to  said
          committee -- recommitted to the Committee on Health in accordance with
          Senate  Rule  6,  sec.  8  --  reported favorably from said committee,
          ordered to first and second report, ordered to a third reading, passed
          by Senate and delivered to the Assembly, recalled, vote  reconsidered,
          restored  to  third  reading, amended and ordered reprinted, retaining
          its place in the order of third reading
 
        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:
 
         EXPLANATION--Matter in italics (underscored) is new; matter in brackets
                              [ ] is old law to be omitted.
                                                                   LBD01972-09-6

        S. 5939--C                          2
 
     1    3. Prescriptions. (a) A pharmacy benefit manager may not substitute or
     2  cause the substituting of one prescription drug for another in  dispens-
     3  ing  a  prescription,  or  alter or cause the altering of the terms of a
     4  prescription, except with the approval of the prescriber or as explicit-
     5  ly required or permitted by law, including regulations of the department
     6  of  financial  services  or the department of health. The superintendent
     7  and commissioner, in coordination with each  other,  are  authorized  to
     8  promulgate  regulations  to  determine when substitution of prescription
     9  drugs may be required or permitted.
    10    (b) To the extent permitted under  federal  law,  a  pharmacy  benefit
    11  manager  shall  pay  a participating pharmacy at minimum at the national
    12  average drug acquisition cost (NADAC) rate or at the  pharmacy  acquisi-
    13  tion  cost  rate  if  there  is  not  a  NADAC rate, plus a professional
    14  dispensing fee that is at minimum the professional dispensing  fee  paid
    15  under  the  state  medical  assistance  program. For generic, brand name
    16  medications, biologic products, or drugs produced through genetic  tech-
    17  nology  or  biopharmaceutical processes as required by a manufacturer, a
    18  federal or state regulatory agency, or  accrediting  body  that  require
    19  unique handling, distribution or administration, in-depth patient teach-
    20  ing,  coordination  of care, or frequent or special monitoring to ensure
    21  successful use,  special  packaging,  shipping  or  other  costs  to  be
    22  incurred by the pharmacy for the dispensing process that is greater than
    23  the  professional  dispensing  fee  paid by the state medical assistance
    24  program, participating pharmacies shall be paid a professional  dispens-
    25  ing  fee  for these costs to ensure a participating pharmacy is not paid
    26  less than its cost to acquire and  dispense  medications.    A  pharmacy
    27  benefit manager shall not pay a participating pharmacy below its pharma-
    28  cy  acquisition  cost but may require demonstration of such cost through
    29  the provision of pharmacy invoices. Provided,  however,  this  paragraph
    30  shall  not  apply  to prescriptions, prescription drugs, or payments for
    31  prescription drugs, distributed, or paid for in whole or in part,  by  a
    32  trust   fund  established  or  maintained  under  the  Labor  Management
    33  Relations Act (29 U.S. Code § 186), pursuant to coverage required by the
    34  terms of a collective bargaining agreement between  an  employer  and  a
    35  labor  organization or certified employee organization; or pursuant to a
    36  health plan, welfare fund, pharmaceutical plan, or other form of medical
    37  or prescription coverage  established,  adopted,  utilized,  funded,  or
    38  agreed upon by an employer and a labor organization or certified employ-
    39  ee organization pursuant to a collective bargaining agreement; or, where
    40  the plan, coverage, fund, or program has been collectively bargained and
    41  pertains  to  a sponsored multi-employer plan, including but not limited
    42  to, plans developed under article five-G of the general  municipal  law,
    43  articles  forty-four  and forty-seven of the insurance law, or any plans
    44  created pursuant to  the  Internal  Revenue  Code,  Employee  Retirement
    45  Income Security Act or any applicable federal statute that provides such
    46  benefits to employee and retiree groups.
    47    §  3.  The  opening paragraph of subdivision 4 of section 280-a of the
    48  public health law, as added by chapter 828  of  the  laws  of  2021,  is
    49  amended to read as follows:
    50    A  pharmacy benefit manager shall, with respect to contracts between a
    51  pharmacy benefit manager and a pharmacy or,  alternatively,  a  pharmacy
    52  benefit  manager  and a pharmacy's contracting agent, such as a pharmacy
    53  services administrative organization, include a  reasonable  process  to
    54  appeal, investigate and resolve disputes regarding multi-source generic,
    55  brand  name,  and  biologic  product, and drugs produced through genetic

        S. 5939--C                          3
 
     1  technology or biopharmaceutical  processes  drug  pricing.  The  appeals
     2  process shall include the following provisions:
     3    §  4.  Section  2911  of  the insurance law is amended by adding a new
     4  subsection (d) to read as follows:
     5    (d) To the extent permitted under  federal  law,  a  pharmacy  benefit
     6  manager  shall  pay  a participating pharmacy at minimum at the national
     7  average drug acquisition cost (NADAC) rate, as  defined  in  subdivision
     8  one  of section two hundred eighty-a of the public health law, or at the
     9  pharmacy acquisition cost rate, as defined in subdivision one of section
    10  two hundred eighty-a of the public health law, if there is not  a  NADAC
    11  rate,  plus a professional dispensing fee that is at minimum the profes-
    12  sional dispensing fee paid under the state medical  assistance  program.
    13  For  generic,  brand  name  medications,  biologic  products,  or  drugs
    14  produced through genetic technology or  biopharmaceutical  processes  as
    15  required  by  a  manufacturer,  a federal or state regulatory agency, or
    16  accrediting body that require unique handling, distribution or  adminis-
    17  tration, in-depth patient teaching, coordination of care, or frequent or
    18  special monitoring to ensure successful use, special packaging, shipping
    19  or other costs to be incurred by the pharmacy for the dispensing process
    20  that  is  greater than the professional dispensing fee paid by the state
    21  medical assistance program, participating pharmacies  shall  be  paid  a
    22  professional  dispensing  fee  for these costs to ensure a participating
    23  pharmacy is not paid less than its cost to acquire and dispense  medica-
    24  tions. A pharmacy benefit manager shall not pay a participating pharmacy
    25  below  its  pharmacy  acquisition  cost but may require demonstration of
    26  such cost through the provision of pharmacy invoices. A pharmacy benefit
    27  manager shall, with respect to  contracts  between  a  pharmacy  benefit
    28  manager and a pharmacy or, alternatively, a pharmacy benefit manager and
    29  a  pharmacy's contracting agent, such as a pharmacy services administra-
    30  tive organization, include a reasonable process to  appeal,  investigate
    31  and resolve disputes regarding multi-source generic, brand name, biolog-
    32  ic  product, and drugs produced through genetic technology or biopharma-
    33  ceutical processes drug pricing. The appeals process shall be considered
    34  within the existing appeals process under section two  hundred  eighty-a
    35  of  the  public health law.  Provided, however, this paragraph shall not
    36  apply to prescriptions, prescription drugs, or payments for prescription
    37  drugs, distributed, or paid for in whole or in part,  by  a  trust  fund
    38  established  or  maintained under the Labor Management Relations Act (29
    39  U.S. Code § 186), pursuant to  coverage  required  by  the  terms  of  a
    40  collective  bargaining  agreement between an employer and a labor organ-
    41  ization or certified employee organization;  or  pursuant  to  a  health
    42  plan,  welfare  fund,  pharmaceutical  plan, or other form of medical or
    43  prescription coverage established, adopted, utilized, funded, or  agreed
    44  upon  by  an  employer  and  a  labor organization or certified employee
    45  organization pursuant to a collective bargaining  agreement;  or,  where
    46  the plan, coverage, fund, or program has been collectively bargained and
    47  pertains  to  a sponsored multi-employer plan, including but not limited
    48  to, plans developed under article five-G of the general  municipal  law,
    49  articles  forty-four  and  forty-seven  of  this  chapter,  or any plans
    50  created pursuant to  the  Internal  Revenue  Code,  Employee  Retirement
    51  Income Security Act or any applicable federal statute that provides such
    52  benefits to employee and retiree groups.
    53    § 5. This act shall take effect January 1, 2027 and shall apply to all
    54  policies  and contracts issued, renewed, modified, altered or amended on
    55  and after such date.
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