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Senate Bill S9497

2025-2026 Legislative Session

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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Current Bill Status - In Senate Committee Finance Committee

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2025-S9497 (ACTIVE) - Details

See Assembly Version of this Bill:
A1428
Current Committee:
Senate Finance
Law Section:
Insurance Law
Laws Affected:
Amd §§3242 & 4329, Ins L
Versions Introduced in 2023-2024 Legislative Session:
A10185

2025-S9497 (ACTIVE) - Summary

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.

2025-S9497 (ACTIVE) - Sponsor Memo

2025-S9497 (ACTIVE) - Bill Text download pdf

                             
                     S T A T E   O F   N E W   Y O R K
 ________________________________________________________________________
 
                                   9497
 
                             I N  S E N A T E
 
                              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:

   Section  1.  Section  3242 of the insurance law is amended by adding a
 new subsection (d) to read as follows:
   (D) (1) AS USED IN THIS SUBSECTION:
   (A) "ELIGIBLE PRESCRIPTION DRUG" MEANS A  PRESCRIPTION  DRUG  APPROVED
 UNDER 21 U.S.C. 355(C) THAT IS NOT UNDER PATENT.
   (B) "GENERIC DRUG" MEANS A DRUG THAT IS APPROVED PURSUANT TO AN APPLI-
 CATION REFERENCING AN ELIGIBLE PRESCRIPTION DRUG THAT IS SUBMITTED UNDER
 SUBSECTION  (J)  OF  SECTION 505 OF THE FEDERAL FOOD, DRUG, AND COSMETIC
 ACT, 21 U.S.C. 355.
   (C) "SUPPLY ISSUE" MEANS A DRUG SHORTAGE OR MEANINGFUL  DISRUPTION  AS
 DEFINED IN 21 U.S.C. 356(C).
   (2)  IN  THE  EVENT  AN AB-RATED GENERIC EQUIVALENT OR INTERCHANGEABLE
 BIOLOGICAL PRODUCT FOR AN ELIGIBLE PRESCRIPTION DRUG IS  COVERED  IN  AN
 INSURER'S  FORMULARY AND SUCH GENERIC DRUG EQUIVALENT IS UNAVAILABLE DUE
 TO A SUPPLY ISSUE WHICH HAS BEEN RECOGNIZED BY THE FEDERAL FOOD AND DRUG
 ADMINISTRATION PURSUANT TO 21 U.S.C.  356E  AND  THE  DOSAGE  CANNOT  BE
 ADJUSTED,  AN INSURER THAT DELIVERS OR ISSUES FOR DELIVERY IN THIS STATE
 A POLICY THAT PROVIDES COVERAGE FOR  PRESCRIPTION  DRUGS  SHALL  PROVIDE
 COVERAGE  FOR  A BRAND NAME ELIGIBLE PRESCRIPTION DRUG TO AN INSURED WHO
 IS ALREADY RECEIVING SUCH PRESCRIPTION DRUG AS A GENERIC  EQUIVALENT  OR
 HAS BEEN DIAGNOSED WITH OR PRESENTED WITH A CONDITION ON OR PRIOR TO THE
 START  OF  THE  PLAN  YEAR THAT IS TREATED BY SUCH ELIGIBLE PRESCRIPTION
 DRUG OR IS AN ELIGIBLE PRESCRIPTION DRUG THAT IS OR WOULD BE PART OF THE
 INSURED'S TREATMENT REGIMEN FOR SUCH CONDITION. SUCH BRAND NAME ELIGIBLE
 PRESCRIPTION DRUG SHALL BE COVERED AT THE SAME LEVEL OF COVERAGE AS  THE
 GENERIC  DRUG  IN  THE INSURER'S FORMULARY UNTIL SUCH TIME AS THE SUPPLY
 ISSUE IS RESOLVED AND THE DRUG HAS BEEN REMOVED FROM  THE  FEDERAL  FOOD
 AND DRUG ADMINISTRATION'S SHORTAGE LIST.
 
  EXPLANATION--Matter in ITALICS (underscored) is new; matter in brackets
                       [ ] is old law to be omitted.
              

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