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S09497 Summary:

BILL NOS09497
 
SAME ASSAME AS A01428
 
SPONSORFERNANDEZ
 
COSPNSR
 
MLTSPNSR
 
Amd §§3242 & 4329, Ins L
 
Requires insurers to cover the substitution of a brand name prescription drug when the federal food and drug administration has declared that there is a supply issue with a generic drug.
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S09497 Text:



 
                STATE OF NEW YORK
        ________________________________________________________________________
 
                                          9497
 
                    IN SENATE
 
                                     March 18, 2026
                                       ___________
 
        Introduced by Sen. FERNANDEZ -- read twice and ordered printed, and when
          printed to be committed to the Committee on Insurance
 
        AN  ACT  to  amend  the insurance law, in relation to substituting brand
          name prescription drugs in the case of a drug shortage
 
          The People of the State of New York, represented in Senate and  Assem-
        bly, do enact as follows:

     1    Section  1.  Section  3242 of the insurance law is amended by adding a
     2  new subsection (d) to read as follows:
     3    (d) (1) As used in this subsection:
     4    (A) "Eligible prescription drug" means a  prescription  drug  approved
     5  under 21 U.S.C. 355(c) that is not under patent.
     6    (B) "Generic drug" means a drug that is approved pursuant to an appli-
     7  cation referencing an eligible prescription drug that is submitted under
     8  subsection  (j)  of  Section 505 of the Federal Food, Drug, and Cosmetic
     9  Act, 21 U.S.C. 355.
    10    (C) "Supply issue" means a drug shortage or meaningful  disruption  as
    11  defined in 21 U.S.C. 356(c).
    12    (2)  In  the  event  an AB-rated generic equivalent or interchangeable
    13  biological product for an eligible prescription drug is  covered  in  an
    14  insurer's  formulary and such generic drug equivalent is unavailable due
    15  to a supply issue which has been recognized by the federal food and drug
    16  administration pursuant to 21 U.S.C.  356e  and  the  dosage  cannot  be
    17  adjusted,  an insurer that delivers or issues for delivery in this state
    18  a policy that provides coverage for  prescription  drugs  shall  provide
    19  coverage  for  a brand name eligible prescription drug to an insured who
    20  is already receiving such prescription drug as a generic  equivalent  or
    21  has been diagnosed with or presented with a condition on or prior to the
    22  start  of  the  plan  year that is treated by such eligible prescription
    23  drug or is an eligible prescription drug that is or would be part of the
    24  insured's treatment regimen for such condition. Such brand name eligible
    25  prescription drug shall be covered at the same level of coverage as  the
    26  generic  drug  in  the insurer's formulary until such time as the supply
    27  issue is resolved and the drug has been removed from  the  federal  food
    28  and drug administration's shortage list.
 
         EXPLANATION--Matter in italics (underscored) is new; matter in brackets
                              [ ] is old law to be omitted.
                                                                   LBD03949-01-5

        S. 9497                             2
 
     1    §  2.  Section  4329  of  the insurance law is amended by adding a new
     2  subsection (d) to read as follows:
     3    (d) (1) As used in this subsection:
     4    (A)  "Eligible  prescription  drug" means a prescription drug approved
     5  under 21 U.S.C. 355(c) that is not under patent.
     6    (B) "Generic drug" means a drug that is approved pursuant to an appli-
     7  cation referencing an eligible prescription drug that is submitted under
     8  subsection (j) of Section 505 of the Federal Food,  Drug,  and  Cosmetic
     9  Act, 21 U.S.C. 355.
    10    (C)  "Supply  issue" means a drug shortage or meaningful disruption as
    11  defined in 21 U.S.C. 356(c).
    12    (2) In the event an AB-rated  generic  equivalent  or  interchangeable
    13  biological  product  for  an eligible prescription drug is covered in an
    14  insurer's formulary and such generic drug equivalent is unavailable  due
    15  to a supply issue which has been recognized by the federal food and drug
    16  administration  pursuant  to  21  U.S.C.  356e  and the dosage cannot be
    17  adjusted, a corporation subject to the provisions of this  article  that
    18  issues  a  contract  that provides coverage for prescription drugs shall
    19  provide coverage for a brand  name  eligible  prescription  drug  to  an
    20  insured  who  is  already  receiving such prescription drug as a generic
    21  equivalent or has been diagnosed with or presented with a  condition  on
    22  or  prior to the start of the plan year that is treated by such eligible
    23  prescription drug or is an eligible prescription drug that is  or  would
    24  be  part  of  the  insured's  treatment regimen for such condition. Such
    25  brand name eligible prescription drug shall be covered at the same level
    26  of coverage as the generic drug in the insurer's  formulary  until  such
    27  time  as the supply issue is resolved and the drug has been removed from
    28  the federal food and drug administration's shortage list.
    29    § 3. This act shall take effect immediately.
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