S. 2554Senate115th Congress (2017-2019)Enacted

Patient Right to Know Drug Prices Act

Introduced March 14, 2018

AI-Generated Summary

Updated April 15, 2026 at 8:57 PM UTC

The Patient Right to Know Drug Prices Act stops health insurers and group health plans from blocking pharmacies or pharmacy‑benefit managers from telling patients how much they would pay out‑of‑pocket for a prescription compared with the cash price without insurance. It also updates Medicare drug‑pricing rules to include clear definitions and reporting requirements for biosimilar biological products, putting them on the same footing as generic drugs.

Key Provisions

  • Health insurers and group health plans may not prevent a pharmacy from informing a patient of the price difference between the patient’s out‑of‑pocket cost under the plan and the cash price of the drug.
  • Plans must also ensure any pharmacy‑benefit manager they contract with does not impose the same restriction on pharmacies.
  • The law defines “out‑of‑pocket cost” as the amount the enrollee pays, including deductibles, copayments, coinsurance, and other expenditures as set by the Secretary.
  • Adds definitions for “biosimilar biological product,” “biosimilar biological product applicant,” “biosimilar biological product application,” and “reference product” to Medicare drug‑pricing statutes.
  • Requires biosimilar applicants to file agreements (similar to generic drug agreements) before the first commercial marketing of the biosimilar, and sets a 1‑year exclusivity period for biosimilar applications.
  • Amends multiple sections of the Medicare Prescription Drug, Improvement, and Modernization Act to treat biosimilars the same way as generic drugs in reporting and agreement rules.

Legislative Activity

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18 earlier actions
Became Law Latest Action

Became Public Law No: 115-263.

October 10, 2018

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SenateIntro Referral

Introduced in Senate

March 14, 2018

SenateIntro Referral

Read twice and referred to the Committee on Health, Education, Labor, and Pensions.

March 14, 2018

SenateCommittee

Committee on Health, Education, Labor, and Pensions. Ordered to be reported with an amendment in the nature of a substitute favorably.

July 25, 2018

SenateCommittee

Committee on Health, Education, Labor, and Pensions. Reported by Senator Alexander with an amendment in the nature of a substitute. Without written report.

July 31, 2018

SenateCalendars

Placed on Senate Legislative Calendar under General Orders. Calendar No. 549.

July 31, 2018

SenateFloor

Measure laid before Senate by unanimous consent. (consideration: CR S6179-6180)

September 17, 2018

SenateFloor

Passed Senate with an amendment by Yea-Nay Vote. 98 - 2. Record Vote Number: 209.

September 17, 2018

SenateFloor

Message on Senate action sent to the House.

September 18, 2018

HouseFloor

Received in the House.

September 20, 2018 • 9:32 AM

HouseFloor

Held at the desk.

September 20, 2018 • 12:28 PM

HouseFloor

Mr. Carter (GA) moved to suspend the rules and pass the bill.

September 25, 2018 • 4:05 PM

HouseFloor

Considered under suspension of the rules. (consideration: CR H8795-8799)

September 25, 2018 • 4:05 PM

HouseFloor

DEBATE - The House proceeded with forty minutes of debate on S. 2554.

September 25, 2018 • 4:05 PM

SenateFloor

Passed/agreed to in House: On motion to suspend the rules and pass the bill Agreed to by voice vote.(text: CR H8795-8796)

September 25, 2018 • 4:26 PM

HouseFloor

On motion to suspend the rules and pass the bill Agreed to by voice vote. (text: CR H8795-8796)

September 25, 2018 • 4:26 PM

HouseFloor

Motion to reconsider laid on the table Agreed to without objection.

September 25, 2018 • 4:26 PM

President

Presented to President.

October 1, 2018

Became Law

Signed by President.

October 10, 2018

Became Law

Became Public Law No: 115-263.

October 10, 2018

Amendments

1 amendment

Offered to this bill

Floor Debate

22 members

What members said about S. 2554 on the floor

9 Republicans12 Democrats1 Independent
Rob Portman
Sen. Rob PortmanR-OH · Sep 17, 2018

Madam President, my colleague from Maryland spoke earlier about the opioid crisis and the fact that we are about to vote on legislation tonight that is called the Opioid Crisis Response Act. He…

Edward J. Markey
Sen. Edward J. MarkeyD-MA · Sep 17, 2018

Mr. President, I ask unanimous consent that the order for the quorum call be rescinded. Mr. President, I rise today to speak about the pending legislation to address the opioid epidemic--a crisis the…

Charles E. Schumer
Sen. Charles E. SchumerD-NY · Sep 17, 2018

Madam President, over the past few days, new allegations have come to light about President Trump's nominee to the Supreme Court, Brett Kavanaugh. These allegations ought to be treated with the…

Benjamin L. Cardin
Sen. Benjamin L. CardinD-MD · Sep 17, 2018

Mr. President, shortly we are going to have an opportunity to vote on the Opioid Crisis Response Act of 2018, which I strongly support. But I want to share with my colleagues a roundtable discussion…

Orrin G. Hatch
Sen. Orrin G. HatchR-UT · Sep 17, 2018

Mr. President, I rise today to speak on three very important topics: first, today's celebration of Constitution Day; second, the signing of the Miscellaneous Tariff Bill Act; and finally, tonight's…

Show 8 more
Susan M. Collins
Sen. Susan M. CollinsR-ME · Sep 17, 2018

Madam President, I rise in support of the Patient Right to Know Drug Prices Act, which is legislation that I have introduced with Senators McCaskill, Barrasso, Stabenow, and Cassidy. Our bill has…

Lamar Alexander
Sen. Lamar AlexanderR-TN · Sep 17, 2018

Mr. President, I ask unanimous consent that the order for the quorum call be rescinded. Mr. President, this morning, in Nashville, as I got on the plane, the headlines were not about tweets or…

Margaret Wood Hassan
Sen. Margaret Wood HassanD-NH · Sep 17, 2018

Mr. President, I thank my colleagues Senator King and Senator Markey for their remarks and their work as we all come together to battle this terrible opioid epidemic. I rise as the Senate considers…

Mitch McConnell
Sen. Mitch McConnellR-KY · Sep 17, 2018

Mr. President, since the Senate last convened, Hurricane Florence made landfall on our Nation's eastern seaboard. According to the latest estimates, this terrible storm has already claimed more than…

Susan M. Collins
Sen. Susan M. CollinsR-ME · May 15, 2018

Mr. President, I rise today in support of legislation I have introduced with several of my colleagues--Senators Murkowski, Barrasso, Stabenow, and Cassidy--that would remove a barrier that prevents…

Dianne Feinstein
Sen. Dianne FeinsteinD-CA · Sep 17, 2018

Madam President, eight Americans die of a drug overdose every hour. In 2016, more Americans died from drug overdoses than during the entire Vietnam war. The 2017 figures are even worse. Preliminary…

Lloyd Doggett
Rep. Lloyd DoggettD-TX-35 · Sep 25, 2018

Madam Speaker, unfortunately, there is just no wonder drug that will cure prescription price gouging. And with many prices for drugs rising at 10 times the rate of inflation, and with an unaffordable…

Maria Cantwell
Sen. Maria CantwellD-WA · Sep 17, 2018

Madam President, I ask unanimous consent that the order for the quorum call be rescinded. Madam President, I come to the floor to thank my colleagues for working so hard on this very important…

Show 11 more
Joe Manchin III
Sen. Joe Manchin IIID-WV · Sep 17, 2018

Mr. President, I first want to thank the good Senator from Tennessee, Lamar Alexander, for basically shepherding this through and working in a bipartisan way. It is a most important piece of…

Claire McCaskill
Sen. Claire McCaskillD-MO · Sep 17, 2018

Thank you, Madam President. I thank my friend and colleague, the Senator from Maine. It is always such a pleasure to work with her on legislation because she is a Senator who does her homework. Don't…

Gary C. Peters
Sen. Gary C. PetersD-MI · Sep 17, 2018

Mr. President, I ask unanimous consent that the order for the quorum call be rescinded. Mr. President, our Nation is suffering through a public health crisis. Our Nation, our neighbors, our…

John Barrasso
Sen. John BarrassoR-WY · Sep 17, 2018

Madam President, I also come to speak on this important piece of legislation and in favor of this important piece of legislation. I just visited with Senator Collins, who knows--as so many Members of…

Michael C. Burgess
Rep. Michael C. BurgessR-TX-26 · Sep 25, 2018

Madam Speaker, I move to suspend the rules and pass the bill (S. 2553) to amend title XVIII of the Social Security Act to prohibit health plans and pharmacy benefit managers from restricting…

Lloyd Doggett
Rep. Lloyd DoggettD-TX-35 · Sep 25, 2018

Mr. Speaker, I thank the gentleman for yielding. Mr. Speaker, I continue to hear from neighbors in my part of Texas and beyond who are unable to afford their prescription drugs, lifesaving drugs.…

Mike Lee
Sen. Mike LeeR-UT · Sep 17, 2018

Mr. President, I ask unanimous consent to complete my brief remarks. Mr. President, Americans know all too well the crippling costs of healthcare in our country today. On top of the daily struggles…

Richard J. Durbin
Sen. Richard J. DurbinD-IL · Sep 17, 2018

Madam President, our Nation is in the midst of the worst drug epidemic in its history. There is no town too small, no suburb too wealthy to be spared. Every day, more than 115 Americans die from an…

Earl L. "Buddy" Carter
Rep. Earl L. "Buddy" CarterR-GA-1 · Sep 25, 2018

Madam Speaker, I move to suspend the rules and pass the bill (S. 2554) to ensure that health insurance issuers and group health plans do not prohibit pharmacy providers from providing certain…

Patty Murray
Sen. Patty MurrayD-WA · Sep 17, 2018

Madam President, I have heard from people across Washington State about the need to respond to the opioid crisis and its tragic impact on so many families and communities. I have visited with people…

Angus S. King Jr.
Sen. Angus S. King Jr.I-ME · Sep 17, 2018

Mr. President, the discussion today is about the opioid crisis, one of the most serious public health crises I have seen in my adult life, certainly in the State of Maine. It is an enormous problem…

Bill Text

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One Hundred Fifteenth Congress of the United States of America

2d Session

Begun and held at the City of Washington on Wednesday, the third day of January, two thousand and eighteen

S. 2554

AN ACT

To ensure that health insurance issuers and group health plans do not prohibit pharmacy providers from providing certain information to enrollees.

1.

Short title

This Act may be cited as the Patient Right to Know Drug Prices Act.

2.

Prohibition on limiting certain information on drug prices

Subpart II of part A of title XXVII of the Public Health Service Act (42 U.S.C. 300gg–11 et seq.) is amended by adding at the end the following:

2729.

Information on prescription drugs

(a)

In general

A group health plan or a health insurance issuer offering group or individual health insurance coverage shall—

(1)

not restrict, directly or indirectly, any pharmacy that dispenses a prescription drug to an enrollee in the plan or coverage from informing (or penalize such pharmacy for informing) an enrollee of any differential between the enrollee's out-of-pocket cost under the plan or coverage with respect to acquisition of the drug and the amount an individual would pay for acquisition of the drug without using any health plan or health insurance coverage; and

(2)

ensure that any entity that provides pharmacy benefits management services under a contract with any such health plan or health insurance coverage does not, with respect to such plan or coverage, restrict, directly or indirectly, a pharmacy that dispenses a prescription drug from informing (or penalize such pharmacy for informing) an enrollee of any differential between the enrollee's out-of-pocket cost under the plan or coverage with respect to acquisition of the drug and the amount an individual would pay for acquisition of the drug without using any health plan or health insurance coverage.

(b)

Definition

For purposes of this section, the term out-of-pocket cost, with respect to acquisition of a drug, means the amount to be paid by the enrollee under the plan or coverage, including any cost-sharing (including any deductible, copayment, or coinsurance) and, as determined by the Secretary, any other expenditure.

.

3.

Modernizing the reporting of biological and biosimilar products

Subtitle B of title XI of the Medicare Prescription Drug, Improvement, and Modernization Act of 2003 (Public Law 108–173) is amended—

(1)

in section 1111—

(A)

by redesignating paragraphs (3) through (8) as paragraphs (6) through (11), respectively;

(B)

by inserting after paragraph (2) the following:

(3)

Biosimilar biological product

The term biosimilar biological product means a biological product for which an application under section 351(k) of the Public Health Service Act is approved.

(4)

Biosimilar biological product applicant

The term biosimilar biological product applicant means a person who has filed or received approval for a biosimilar biological product under section 351(k) of the Public Health Service Act.

(5)

Biosimilar biological product application

The term biosimilar biological product application means an application for licensure of a biological product under section 351(k) of the Public Health Service Act.

;

(C)

in paragraph (6), as so redesignated, by inserting , or a biological product for which an application is approved under section 351(a) of the Public Health Service Act before the period;

(D)

in paragraph (7), as so redesignated—

(i)

by striking paragraph (3) and inserting paragraph (6);

(ii)

by inserting or a reference product in a biosimilar biological product application after ANDA; and

(iii)

by inserting or under section 351(a) of the Public Health Service Act before the period; and

(E)

by adding at the end the following:

(12)

Reference product

The term reference product means a brand name drug for which a license is in effect under section 351(a) of the Public Health Service Act.

;

(2)

in section 1112—

(A)

in subsection (a)—

(i)

in paragraph (1)—

(I)

by inserting or a biosimilar biological product applicant who has submitted a biosimilar biological product application for which a statement under section 351(l)(3)(B)(ii)(I) of the Public Health Service Act has been provided after Federal Food, Drug, and Cosmetic Act; and

(II)

by inserting or the biosimilar biological product that is the subject of the biosimilar biological product application, as applicable after the ANDA; and

(ii)

in paragraph (2)—

(I)

in the matter preceding subparagraph (A), by inserting or a biosimilar biological product applicant after generic drug applicant;

(II)

in subparagraph (A)—

(aa)

by striking marketing and inserting marketing,; and

(bb)

by inserting or the reference product in the biosimilar biological product application before involved;

(III)

in subparagraph (B), by inserting or of the biosimilar biological product for which the biosimilar biological product application was submitted after submitted; and

(IV)

by amending subparagraph (C) to read as follows:

(C)

as applicable—

(i)

the 180-day period referred to in section 505(j)(5)(B)(iv) of the Federal Food, Drug, and Cosmetic Act as it applies to such ANDA or to any other ANDA based on the same brand name drug; or

(ii)

the 1-year period referred to in section 351(k)(6)(A) of the Public Health Service Act as it applies to such biosimilar biological product application or to any other biosimilar biological product application based on the same brand name drug.

; and

(B)

in subsection (b)—

(i)

by amending paragraph (1) to read as follows:

(1)

Requirement

(A)

Generic drugs

A generic drug applicant that has submitted an ANDA containing a certification under section 505(j)(2)(A)(vii)(IV) of the Federal Food, Drug, and Cosmetic Act with respect to a listed drug and another generic drug applicant that has submitted an ANDA containing such a certification for the same listed drug shall each file the agreement in accordance with subsection (c). The agreement shall be filed prior to the date of the first commercial marketing of either of the generic drugs for which such ANDAs were submitted.

(B)

Biosimilar biological products

A biosimilar biological product applicant that has submitted a biosimilar biological product application for which a statement under section 351(l)(3)(B)(ii)(I) of the Public Health Service Act has been provided with respect to a reference product and another biosimilar biological product applicant that has submitted a biosimilar biological product application for which such a statement for the same reference product has been provided shall each file the agreement in accordance with subsection (c). The agreement shall be filed prior to the date of the first commercial marketing of either of the biosimilar biological products for which such biosimilar biological product applications were submitted.

; and

(ii)

in paragraph (2)—

(I)

by striking between two generic drug applicants is an agreement and inserting is, as applicable, an agreement between 2 generic drug applicants; and

(II)

by inserting , or an agreement between 2 biosimilar biological product applicants regarding the 1-year period referred to in section 351(k)(6)(A) of the Public Health Service Act as it applies to the biosimilar biological product applications with which the agreement is concerned before the period;

(3)

in section 1115, by striking or generic drug applicant each place such term appears and inserting , generic drug applicant, or biosimilar biological product applicant; and

(4)

in section 1117, by striking , or any agreement between generic drug applicants and inserting or a biosimilar biological product applicant, any agreement between generic drug applicants, or any agreement between biosimilar biological product applicants.

Speaker of the House of Representatives

Vice President of the United States and President of the Senate