Ohio 2025-2026 Regular Session

Ohio Senate Bill SB160 Latest Draft

Bill / Introduced Version

                            As Introduced
136th General Assembly
Regular Session	S. B. No. 160
2025-2026
Senators Liston, Johnson
A B I L L
To enact section 3902.65 of the Revised Code 
regarding prescription drugs and medication 
switching.
BE IT ENACTED BY THE GENERAL ASSEMBLY OF THE STATE OF OHIO:
Section 1. That section 3902.65 of the Revised Code be 
enacted to read as follows:
Sec. 3902.65.  	(A) As used in this section: 
(1) "Interchangeable biological product" and "generically 
equivalent drug" have the same meanings as in section 3715.01 of 
the Revised Code.
(2) "Pharmacy" has the same meaning as in section 4729.01 
of the Revised Code.
(3) "Rate of inflation" has the same meaning as in section 
107.032 of the Revised Code.
(4) "Wholesale acquisition cost" has the same meaning as 
in 42 U.S.C. 1395w-3a. 
(B) Notwithstanding section 3901.71 of the Revised Code, 
but subject to divisions (C) and (D) of this section, with 
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As Introduced
regard to health benefit plans amended, issued, or renewed on or 
after the effective date of this section, a health plan issuer 
shall not do any of the following during a plan year:
(1) Increase a covered person's burden of cost-sharing 
with respect to a drug; 
(2) Move a drug to a more restrictive tier of a health 
benefit plan's formulary; 
(3) Remove a drug from a health benefit plan's formulary 
unless one of the following occurred: 
(a) The United States food and drug administration issued 
a statement about the drug calling into question the clinical 
safety of the drug. 
(b) The drug manufacturer notified the United States food 
and drug administration of a permanent discontinuance or 
interruption of the manufacture of the drug as required by 21 
U.S.C. 356c. 
(c) The drug manufacturer has removed the drug from sale 
in the United States. 
(4) Limit or reduce coverage of a drug with respect to a 
covered person in any other way, including subjecting it to a 
prior authorization requirement. 
(C) This section shall not be construed to do any of the 
following: 
(1) Prevent a health plan issuer from adding a drug to its 
formulary; 
(2) Prevent a health plan issuer from removing a drug from 
its formulary if the drug manufacturer has removed the drug from 
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As Introduced
sale in the United States; 
(3) Prevent a health care provider from prescribing 
another drug covered by the health benefit plan that the 
provider considers medically appropriate for the covered person; 
(4) In the case of a prescribed drug for which a 
generically equivalent drug or interchangeable biological 
product is available, prevent any of the following: 
(a) A pharmacist from substituting the generically 
equivalent drug or interchangeable biological product for the 
prescribed drug in accordance with section 4729.38 of the 
Revised Code; 
(b) A health plan issuer from requiring a covered person 
to use the generically equivalent drug or interchangeable 
biological product instead of the prescribed drug, even when the 
equivalent or product becomes available during a plan year; 
(c) A covered person from using the generically equivalent 
drug or interchangeable drug product instead of the prescribed 
drug, even when the equivalent or product becomes available 
during a plan year. 
(5) Prevent a pharmacist from substituting for a 
prescribed epinephrine autoinjector another epinephrine 
autoinjector pursuant to section 4729.382 of the Revised Code.
(D) If, at any point during a plan year, the wholesale 
acquisition cost for a drug increases by more than five per cent 
plus the rate of inflation, as compared to the average wholesale 
acquisition cost for the previous plan year, division (C) of 
this section does not apply to that drug for the remainder of 
the plan year.
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As Introduced
(E) A violation of this section shall be considered an 
unfair and deceptive practice in the business of insurance for 
the purposes of section 3901.21 of the Revised Code. 
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