S.Amdt. 2726Senate118th Congress (2023-2025)
S.Amdt. 2726
Sponsored by
Sen. Jeff Merkley (D-OR)
Submitted July 11, 2024
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Senate amendment submitted
July 11, 2024
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Submitted
SA 2726. Mr. MERKLEY (for himself and Mr. Welch) submitted an amendment intended to be proposed by him to the bill S. 4638, to authorize appropriations for fiscal year 2025 for military activities of the Department of Defense, for military construction, and for defense activities of the Department of Energy, to prescribe military personnel strengths for such fiscal year, and for other purposes; which was ordered to lie on the table; as follows: At the appropriate place in title VII, insert the following: SEC. 7__. REFERENCE PRICES FOR PRESCRIPTION DRUGS UNDER THE TRICARE PROGRAM. (a) In General.--Each year, the Secretary of Defense shall establish the reference price for each prescription drug provided to beneficiaries under the TRICARE program-- (1) by determining the lowest retail list price for the drug among the countries specified in subsection (b) in which the drug is available, if drug pricing information is available for at least 3 of such countries; or (2) in the case of a drug for which drug pricing information or dosage equivalents are not available for at least 3 of such countries, by determining an appropriate price based on the determination by the Secretary of-- (A) the added therapeutic effect of the drug; (B) the value of the drug; (C) patient access to the drug; [[Page S5021]] (D) the costs associated with researching and developing the drug; and (E) other factors, as the Secretary determines appropriate. (b) Reference Countries.--The countries specified in this subsection are Japan, Germany, the United Kingdom, France, Italy, Canada, Australia, Spain, the Netherlands, Switzerland, and Sweden. (c) Application Under TRICARE Program.-- (1) Federal supply schedule.--In procuring a prescription drug under the Federal Supply Schedule of the General Services Administration, the Secretary of Defense, and any drug manufacturer providing the prescription drug to the Secretary, shall comply with the price limitations under section 8126 of title 38, United States Code, or the reference price limitations for such drug established under subsection (a), whichever is lower. (2) Contracts with pharmacy benefits managers.-- (A) In general.--In entering into contracts with pharmacy benefits managers to carry out the pharmacy benefits program under section 1074g of title 10, United States Code, the Secretary of Defense shall ensure that the price for prescription drugs provided by such pharmacy benefits managers to beneficiaries under the TRICARE program does not exceed the price for such drug established under the pharmacy benefits program or the reference price for such drug established under subsection (a), whichever is lower. (B) Drug manufacturers.--A drug manufacturer may not sell a prescription drug under the pharmacy benefits program under section 1074g of title 10, United States Code, for an amount that exceeds the limitation under subparagraph (A). (3) Direct purchasing.-- (A) In general.--In making direct purchases of prescription drugs under any authority not covered by paragraph (1) or (2), the Secretary of Defense shall ensure that the price for such drug does not exceed the reference price for such drug established under subsection (a). (B) Drug manufacturers.--A drug manufacturer may not sell a prescription drug to the Secretary of Defense under an authority specified in subparagraph (A) for an amount that exceeds the reference price for such drug established under subsection (a). (d) Enforcement.-- (1) Civil penalty.--A drug manufacturer who does not comply with the requirements under subsection (c) shall be subject to a civil penalty, for each year in which the violation occurs and with respect to each drug for which the violation occurs, in an amount equal to 5 times the difference between-- (A) the total amount received by the manufacturer for sales of the drug under the TRICARE program for the year; less (B) the total amount the manufacturer would have received for sales of the drug under the TRICARE program for the year if the manufacturer had complied with subsection (c). (2) Amounts collected.-- (A) In general.--Each year, the Secretary of the Treasury shall transfer to the Director of the National Institutes of Health an amount equal to the amount collected in civil penalties under subsection (e) for the previous year. (B) Use of amounts.--The Director of the National Institutes of Health shall use amounts transferred under subparagraph (A) for purposes of conducting drug research and development. (e) Applicability to Brand and Generic Drugs.--The reference price established under subsection (a) shall apply to drugs approved under subsection (c) or (j) of section 505 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355) or under subsection (a) or (k) of section 351 of the Public Health Service Act (42 U.S.C. 262). (f) TRICARE Program Defined.--In this section, the term ``TRICARE program'' has the meaning given that term in section 1072 of title 10, United States Code. ______