summary
Introduced
02/04/2026
02/04/2026
In Committee
02/17/2026
02/17/2026
Crossed Over
Passed
Dead
Introduced Session
104th General Assembly
Bill Summary
Creates the 340B Drug Pricing Program Reporting Act. On or before April 1, 2027 and each April 1 thereafter, requires a 340B covered entity to report the specified information and transactions to the Department of Public Health concerning the 340B covered entity's participation in or participation on behalf of the 340B covered entity in the federal 340B Program for the previous calendar year. On or before November 15, 2027 and each November 15 thereafter, requires the Department to prepare a report that aggregates the data submitted; submit the report to the General Assembly in an electronic format; and post the report on the Department's website. Provides that pharmaceutical manufacturers may request a 340B covered entity to provide specified information concerning the dispensation of 340B drugs. Sets forth provisions concerning penalties, exemptions for pharmaceutical manufacturers, and rulemaking. Provides that the Act is repealed on January 1, 2031. Effective immediately.
AI Summary
This bill, titled the 340B Drug Pricing Program Reporting Act, mandates that entities participating in the federal 340B Program, which allows certain healthcare organizations to purchase outpatient drugs at reduced prices, must report detailed information about their participation to the Department of Public Health annually. Specifically, by April 1st each year starting in 2027, these "340B covered entities" (defined as eligible organizations with a service address in Illinois, including their associated child sites or grantees) must submit data on their drug acquisition costs, dispensing payments, payments to contract pharmacies (pharmacies that dispense 340B drugs on behalf of a covered entity), how savings are used for charity care or community benefits, and their overall operating and charity care costs. The Department will then compile this information into a public report by November 15th each year, starting in 2027, and post it online. The bill also outlines penalties for late reporting, allows pharmaceutical manufacturers to request specific dispensing data from covered entities to prevent issues like duplicate discounts or diversion, and includes provisions for rulemaking and an exemption for manufacturers from certain restrictions. This Act will be repealed on January 1, 2031.
Committee Categories
Government Affairs
Sponsors (1)
Last Action
House Executive Committee Hearing (10:00:00 2/25/2026 Room 118) (on 02/25/2026)
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