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Arkansas General Assembly· HB 1531Notification that HB1531 is now Act 630

An act TO PROHIBIT PHARMACEUTICAL MANUFACTURERS FROM 10 RESTRICTING OR LIMITING PRESCRIPTION MEDICATIONS TO A 11 LIMITED DISTRIBUTION NETWORK OF OUT-OF-STATE 12 PHARMACIES, the official text

Shown verbatim: the complete text as captured from the official PDF posted by the Arkansas General Assembly, fetched 2026-07-23. Page and line markers are part of the official record; nothing is edited or removed. The official bill page.
Stricken language would be deleted from and underlined language would be added to present law.

1 State of Arkansas      As Engrossed: H3/18/25 H3/31/25 S4/7/25

2 95th General Assembly               A Bill

3 Regular Session, 2025                                            HOUSE BILL 1531

4

5 By: Representative Achor

6 By: Senator J. Boyd

7

8                           For An Act To Be Entitled

9   AN ACT TO PROHIBIT PHARMACEUTICAL MANUFACTURERS FROM

10  RESTRICTING OR LIMITING PRESCRIPTION MEDICATIONS TO A

11  LIMITED DISTRIBUTION NETWORK OF OUT-OF-STATE

12  PHARMACIES; AND FOR OTHER PURPOSES.

13

14

15                                    Subtitle

16                       TO PROHIBIT PHARMACEUTICAL MANUFACTURERS

17                       FROM RESTRICTING OR LIMITING

18                       PRESCRIPTION MEDICATIONS TO A LIMITED

19                       DISTRIBUTION NETWORK OF OUT-OF-STATE

20                       PHARMACIES.

21

22 BE IT ENACTED BY THE GENERAL ASSEMBLY OF THE STATE OF ARKANSAS:

23

24  SECTION 1. Arkansas Code Title 20, Chapter 64, Subchapter 1, is

25 amended to add an additional section to read as follows:

26  20-64-105. Pharmaceutical manufacturer limited distribution of

27 medication -- Legislative findings -- Definitions.

28  (a) The General Assembly finds that:

29  (1) It is beneficial to this state to support patient access to

30 prescription drugs and pharmacy services in a market that ensures that

31 patients can access safe and effective prescription medications with same day

32 access, as well as patient freedom of choice to utilize local trusted

33 medication experts and state-based local pharmacists who support patients

34 with advice and guidance for safe and effective use of these medications;

35  (2) It may cause harm to patients in this state when local

36 pharmacies, clinics, and hospitals are unable to access prescription

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1 medications from pharmaceutical manufacturers or pharmaceutical wholesalers

2 due to out-of-state limited distribution to pharmacies utilizing:

3                     (A) Pharmacy benefits manager-affiliated mail order

4 pharmacies;

5                     (B) Publicly traded corporation pharmacies;

6                     (C) Pharmaceutical manufacturer-affiliated mail order

7 pharmacies;

8                     (D) Insurance company-affiliated mail order pharmacies; or

9                     (E) Pharmaceutical wholesaler-affiliated mail order

10 pharmacies;

11              (3) The reasons for the limited distribution networks by

12 pharmaceutical manufacturers are not often disclosed or may not operate with

13 optimal patient safety and same day patient access in mind;

14              (4) The supply chain that brings prescription medications from

15 the pharmaceutical manufacturer to the pharmacy is often complex and lacks

16 transparency; and

17              (5) Having more transparency and oversight concerning limited

18 distribution medications would:

19                    (A) Protect patients with better and more stable

20 prescription drug inventory for both immediate and long-term patient care

21 needs; and

22                    (B) Better respond to future national security threats and

23 natural disasters in this state.

24  (b) As used in this section:

25              (1) "Pharmaceutical manufacturer" means a business or entity

26 that makes, processes, or packages prescription drugs, over-the-counter

27 medications, or medical devices to sell in pharmacies or other healthcare

28 facilities, including any activities that manipulate, test, or control the

29 product or process;

30              (2) "Pharmaceutical manufacturer for Medicaid" means an entity

31 or business that is engaged in manufacturing, preparing, propagating,

32 compounding, processing, packaging, repackaging, or labeling of a

33 prescription drug that is eligible in the Medicaid Drug Rebate Program or

34 agrees to participate in the Medicaid Drug Rebate Program to pay a rebate to

35 states for prescription drugs covered by the Arkansas Medicaid Program; and

36              (3) "State government and public plan sponsor" means an employer

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1 sponsor of a health benefit plan for employees that is established or

2 maintained by:

3                    (A) The Arkansas Municipal League;

4                    (B) A public two-year or four-year institution of higher

5 education, including a community college or technical college;

6                    (C) The Division of Arkansas State Police;

7                    (D) A municipality;

8                    (E) A county; or

9                    (F) Any other plan or program that is funded by a state

10 appropriation to furnish, cover the cost of, or otherwise provide for

11 pharmacist services to an individual who resides in or is employed in this

12 state.

13         (c)(1) A pharmaceutical manufacturer or a pharmaceutical manufacturer

14 for Medicaid that expects for their prescription medications to be eligible,

15 considered for payment, and covered in a state government and public plan

16 sponsor for health benefit plans:

17         (A) Shall have an active wholesale distributor permit active and

18 in good standing with the Arkansas State Board of Pharmacy under � 20-64-505;

19 and

20         (B) Shall not restrict or limit prescription medications more

21 than three (3) months after a launch of a new product to a limited

22 distribution network of pharmacies without having similar access and allowing

23 for upon request or application by pharmacy at least:

24                   (i) A local network of public institution academic medical

25 center access;

26                   (ii) Geographic diversity of access within the state;

27                   (iii) Diverse access for local for-profit and nonprofit

28 pharmacies in good standing with the board and that have experience or

29 accreditation in managing expensive specialty or limited distribution

30 medications; and

31                   (iv) The pharmacy meeting medication specific United

32 States Food and Drug Administration guidance or requirements for:

33                                (a) Proper and safe storage, handling,

34 monitoring, and drug delivery;

35                                (b) Patient or medication data collection,

36 monitoring, or reporting; and

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1                         (c) Patient management services.

2              (2) Subdivision (c)(1) of this section does not apply to the

3 State and Public School Life and Health Insurance Program.

4         (d)(1)(A) A pharmaceutical manufacturer or a pharmaceutical

5 manufacturer for Medicaid that requests for restricted networks for six (6)

6 months or longer shall present the request to the board to explain how the

7 restriction will support and not hinder the mission of the board to promote,

8 preserve, and protect the public health, safety, and welfare of citizens of

9 this state.

10             (B) The request under subdivision (d)(1)(A) of this

11 section shall not be effective until the request is approved by the board.

12             (2)(A) When considering the request under subdivision (d)(1)(A)

13 of this section, the board may consider the following factors for a request

14 of a limited network:

15                        (i) Costs;

16                        (ii) Logistics;

17                        (iii) Patient caseload;

18                        (iv) The rarity of the prescription drug that is

19 used;

20                        (v) The rarity of the disease or condition; and

21                        (vi) Any other factors unique or relevant to the

22 medication and disease or condition treated.

23             (B) The limited network shall allow some pharmacies in

24 this state, upon request or application, to participate and access the

25 medications to meet the needs of patients with same day access in this state

26 without requiring patients to use out-of-state or in-state common mail

27 carriers for access.

28             (3) The board may issue a temporary waiver or temporary limited

29 use allowance for utilization, payment, or coverage of prescription drugs

30 from a pharmaceutical manufacturer or a pharmaceutical manufacturer for

31 Medicaid for coverage and payment for a state government and public plan

32 sponsor for a health benefit plan to protect public health and access.

33             (4) A public hearing of the board shall be called as soon as

34 possible to discuss and approve or deny any request for a permanent limited

35 network or restriction relating to state-based Class A pharmacies with retail

36 permits in good standing with the board.

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1   (e) A state government and public plan sponsor for a health benefit

2 plan shall not pay for prescription drugs from a pharmaceutical manufacturer

3 or a pharmaceutical manufacturer for Medicaid who is noncompliant with this

4 section unless the board has granted a temporary waiver or temporary

5 allowance to protect public health and access.

6   (f) If a pharmaceutical manufacturer or a pharmaceutical manufacturer

7 for Medicaid is not in compliance with this section, the board shall fine the

8 pharmaceutical manufacturer or a pharmaceutical manufacturer for Medicaid ten

9 thousand dollars ($10,000) per day of noncompliance.

10

11  SECTION 2. DO NOT CODIFY. SEVERABILITY CLAUSE. If any provision of

12 this act or the application of this act to any person or circumstance is held

13 invalid, the invalidity shall not affect other provisions or applications of

14 this act which can be given effect without the invalid provision or

15 application, and to this end, the provisions of this act are declared

16 severable.

17

18  SECTION 3. DO NOT CODIFY. TEMPORARY LANGUAGE. Compliance date.

19  A pharmaceutical manufacturer or a pharmaceutical manufacturer for

20 Medicaid shall be in compliance with this act on or before September 1, 2026.

21

22             /s/Achor

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