HB 3086
bill requiring drug makers to report wholesale prices yearly
Died in committee
Verdict: No flags
Initial review · graded Oct 20, 2026 · Headline, summary and grade are analysis of the bill text, not a finding about any person · How we grade
Caption
relating to requirements for pharmaceutical drug manufacturers to report prescription drug costs.
Caption from analyzed text · version I.
Summary
Every FDA-approved drug sold in Texas, reported by January 15.
The bill requires drug makers to send the state health department a yearly report, by January 15, listing the wholesale price of every FDA-approved prescription drug they sell in Texas. For drugs whose price jumped 40 percent or more over three years or 15 percent or more in one year, the maker must also explain why, report research costs, and list recent approvals and patent losses, and the department must post that increase information online within 60 days. It folds the old separate price-increase report into this annual report, and it makes the department's administrative penalty for violations mandatory instead of optional.
Labels
Labels: NEVER GOT A HEARING. Filed Feb 20, 2025 and referred to the House Public Health committee. No public hearing. The bill died.
Receipt
The receipt
89R-HB3086 · 2025-02-20
SOLD BY
ITEM
relating to requirements for pharmaceutical drug manufacturers to report prescription drug costs.
WHAT IT DOES
Every FDA-approved drug sold in Texas, reported by January 15.
The bill requires drug makers to send the state health department a yearly report, by January 15, listing the wholesale price of every FDA-approved prescription drug they sell in Texas. For drugs whose price jumped 40 percent or more over three years or 15 percent or more in one year, the maker must also explain why, report research costs, and list recent approvals and patent losses, and the department must post that increase information online within 60 days. It folds the old separate price-increase report into this annual report, and it makes the department's administrative penalty for violations mandatory instead of optional.
CHARGES
[ ] NONE FOUND
TOTAL
No fiscal note in the loaded record.
HISTORY
- Filed
- Read first time
- Referred to Public Health
FILED UNDER
No verified beat found.
THANK YOU FOR CHECKING THE RECEIPT
CAMPAIGN PAID FOR BY
CAMPAIGN PAID FOR BY
Donors
Donors report through Friends of Tom Oliverson.
Not tied to this bill.
Sources
The author's campaign account only. Own money and internal transfers are separate on the member page.
Derived itemized flow · Oct 27, 2024 to Oct 24, 2026. State data as of Nov 4, 2026.
Derived itemized contributions on live regular reports and uncovered special-session dates. Internal account transfers and daily reports are excluded.
MoneyMissing data does not establish zero giving. Display amounts are rounded.
Votes
No floor vote loaded for this bill.
Fiscal
No fiscal note in the loaded record.
How this was graded
Analysis of text version I by claude-opus-5-5, Oct 20, 2026, against the published rubric.
Sources
Texas House · Filed Feb 20, 2025
03/20/2025 H Referred to Public Health: Mar 20 2025 11:50AM
Texas Legislature Online · Introduced
Data snapshot Oct 26, 2026 at 4:20 AM CDT. Grades, charges, quotes and corrections follow the published record.
House committee · Public Health · Final status: Died in committee
Subjects
Health--General
Health--Other Diseases & Medical Conditions
Occupational Regulation--Health Occupations
MEDICINE & PRESCRIPTION DRUGS
HEALTH & HUMAN SERVICES COMMISSION
STATE HEALTH SERVICES, DEPARTMENT OF
Text
The text as introduced · 489 words
89R8229 JTZ-F By: Oliverson H.B. No. 3086 A BILL TO BE ENTITLED AN ACT relating to requirements for pharmaceutical drug manufacturers to report prescription drug costs. BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS: SECTION 1. Section 441.0051, Health and Safety Code, is amended to read as follows: Sec. 441.0051. ANNUAL REPORT. (a) Not later than the 15th day of each calendar year, a pharmaceutical drug manufacturer shall submit a report to the department stating the current wholesale acquisition cost information for the United States Food and Drug Administration-approved prescription drugs sold in or into this state by that manufacturer. (b) For a prescription drug with a wholesale acquisition cost increase of 40 percent or more over the drug's wholesale acquisition cost in the preceding three calendar years or 15 percent or more in the preceding calendar year, a pharmaceutical drug manufacturer shall include in the annual report required under Subsection (a): (1) information on whether the prescription drug is a brand name drug or generic version of a brand name drug; (2) a statement on each factor that caused the increase in the wholesale acquisition cost and an explanation of the impact of each factor on the cost; (3) aggregate, research, and development costs as filed with United States Securities and Exchange Commission on Form 10-K for the most recent calendar year for which final audit data is available; (4) the name of each of the manufacturer's prescription drugs the United States Food and Drug Administration approved in the previous three calendar years; and (5) the name of each of the manufacturer's prescription drugs that lost patent exclusivity in the United States in the previous three calendar years. (c) The information a pharmaceutical drug manufacturer submits to the department under Subsections (a) and (b) must be consistent with the information the manufacturer includes in the manufacturer's annual consolidated report filed with the United States Securities and Exchange Commission on Form 10-K or any other public disclosure. SECTION 2. Section 441.0054, Health and Safety Code, is amended to read as follows: Sec. 441.0054. PUBLICATION OF COST INCREASE INFORMATION. Not later than the 60th day after receipt of the report submitted under Section 441.0051 [ or 441.0053(a) ], the department shall publish the required cost increase information [ required by Section 441.0053 ] on the department's prescription drug price information Internet website. SECTION 3. Section 441.0102(a), Health and Safety Code, is amended to read as follows: (a) The department shall [ may ] assess an administrative penalty against a person who violates this chapter or a rule adopted under this chapter. SECTION 4. Section 441.0053, Health and Safety Code, is repealed. SECTION 5. As soon as practicable after the effective date of this Act, the executive commissioner of the Health and Human Services Commission shall adopt rules necessary to implement the changes in law made by this Act. SECTION 6. This Act takes effect September 1, 2025.