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Oklahoma Legislature· SB 1306Second Reading referred to Health and Human Services

An act relating to prescription drugs, the official text

Shown verbatim: the complete text as captured from the official PDF posted by the Oklahoma Legislature, fetched 2026-07-23. Page and line markers are part of the official record; nothing is edited or removed. The official bill page.
1                            STATE OF OKLAHOMA

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2                  2nd Session of the 60th Legislature (2026)

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3 SENATE BILL 1306               By: Hicks
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6                            AS INTRODUCED

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7   An Act relating to prescription drugs; defining

7   terms; prohibiting an insurer from modifying coverage

8   under certain conditions; providing certain

8   exceptions; providing for certain civil penalty;

9   requiring promulgation of rules; providing for

9   codification; and providing an effective date.

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12 BE IT ENACTED BY THE PEOPLE OF THE STATE OF OKLAHOMA:
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13  SECTION 1.      NEW LAW  A new section of law to be codified

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14 in the Oklahoma Statutes as Section 6850.2 of Title 36, unless there
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15 is created a duplication in numbering, reads as follows:
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16  A. As used in this section:

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17  1. "Insurer" means an insurer as defined pursuant to Section

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18 6054 of Title 36 of the Oklahoma Statutes;
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19  2. "Practitioner" means a practitioner as defined pursuant to

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20 Section 6054 of Title 36 of the Oklahoma Statutes; and
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21  3. "Prescription drug" or "drug" means a prescription drug as

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22 defined pursuant to Section 367.2 of Title 59 of the Oklahoma
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23 Statutes.
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    Req. No. 2648                                              Page 1
1   B. An insurer shall not modify an insured's coverage of a

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2 prescription drug if the following conditions are met:
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3   1. The drug has been previously preauthorized for coverage by

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4 the insurer or was listed on the formulary of the insurer at the
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5 time the insured was prescribed the drug by his or her practitioner;
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6   2. The insured has already received the drug; and

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7   3. A practitioner continued to prescribe the drug to the

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8 insured.
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9   C. Modification prohibited under this section shall include,

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10 but not be limited to:
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11  1. Increasing the premium, co-payment, coinsurance, or

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12 deductible;
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13  2. Denying or otherwise failing to provide continued coverage

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14 of the prescription drug;
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15  3. Moving the drug to a more restrictive coverage category or

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16 tier; or
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17  4. Replacing the brand-name drug for a generic drug after the

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18 insured has qualified for the brand-name drug pursuant to this
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19 section.
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20  D. Nothing in this section shall be construed to prohibit an

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21 insurer from modifying coverage of a prescription drug if:
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22  1. The United States Food and Drug Administration has issued a

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23 statement calling into question the clinical safety of the drug; or
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    Req. No. 2648                                              Page 2
1   2. The manufacturer of the drug has notified the United States

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2 Food and Drug Administration of a manufacturing discontinuance or
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3 potential discontinuance of the drug, as required by 21 U.S.C.,
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4 Section 356c.
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5   E. Any insurer that violates the provisions of this section

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6 shall be subject to a civil penalty in an amount to be determined by
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7 the Insurance Commissioner. The Insurance Commissioner shall
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8 promulgate rules to effectuate the provisions of this section.
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9   SECTION 2. This act shall become effective November 1, 2026.

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11  60-2-2648      CAD  12/29/2025 9:10:33 AM

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    Req. No. 2648                              Page 3
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