H.R. 6501: Prescription Drug and Medical Device Price Review Board Act of 2016
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H.R. 6501: Prescription Drug and Medical Device Price Review Board Act of 2016
114th Congress · introduced 2016-12-08 · Health · Latest: Referred to the Subcommittee on Courts, Intellectual Property, and the Internet.
federal
Follow this bill, step by step
- Where it came from: introduced 2016-12-08 · official record
- Who proposed it: Rep. DeLauro, Rosa L. [D-CT-3] · what a sponsor is
- What happened next: no floor votes in our records yet. Why?
- Where it stands now: Referred to the Subcommittee on Courts, Intellectual Property, and the Internet. Not final yet: this can still change. We check for updates every day.
- If it becomes law and spends money: follow the money to money laws, then agencies and contracts and grants.
Official title
Prescription Drug and Medical Device Price Review Board Act of 2016
Plain summary
Prescription Drug and Medical Device Price Review Board Act of 2016 This bill establishes the Prescription Drug and Medical Device Price Review Board within the Food and Drug Administration. Each manufacturer of a prescription drug or medical device that is sold in the United States must submit to the board: each type of prescription drug and medical device that it sells in the United States, or in a country that is a member of the Organization for Economic Co-operation and Development; the price charged by the manufacturer for the drug or device; and the costs of the manufacturer to produce them. The board must establish a formula for determining whether the average manufacturer price of a prescription drug or medical device over an annual quarter is an excessive price. Manufacturers may not charge excessive prices. Individuals may petition the board to determine whether the price for a prescription drug or medical device is excessive. The board may subject violators to reduced patent terms, civil penalties, and increased Medicaid rebates. The bill amends the Internal Revenue Code to impose a tax on the sale of prescription drugs or medical devices that have excessive prices. The board must allow individuals to import from approved counties prescription drugs and devices that are comparable to prescription drugs and devices with excessive prices.
Congressional Research Service summary (Introduced in House), quoted unchanged (nonpartisan). Read the source.
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A “Nay” vote
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What does this mean? (plain words)
Official text
Prescription Drug and Medical Device Price Review Board Act of 2016
Source: Congressional Research Service summary (Introduced in House)
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How did my representative vote? · This bill's floor votes
Officials and money
Sponsor: Rep. DeLauro, Rosa L. [D-CT-3] · 8 cosponsors
Cost estimate: No cost estimate published yet.
Cosponsors on this site
Janice D. Schakowsky (D-IL), Lloyd Doggett (D-TX), Gwen Moore (D-WI), Marcy Kaptur (D-OH), Peter Welch (D-VT)
Sponsor's campaign money: Rep. DeLauro, Rosa L. [D-CT-3] reported raising $1.6 million (2025–2026). Details. Shown for context only; it does not mean any donor supported this bill.
No linked floor roll calls in our collected records yet. This does not mean the bill has never had a vote. Check the official bill history.
Words on this page, explained (1)
- Bill
- A proposed law. It becomes law only if it passes the legislature and is signed by the president or governor (or a veto is overridden).
Plain meanings written from linked sources. All words.
Sources
- Congressional Research Service summary (Introduced in House)
- Congress.gov
- Data: GovInfo BILLSTATUS bulk data (Library of Congress), BILLSTATUS-114hr6501.xml <https://www.govinfo.gov/bulkdata/BILLSTATUS/114/hr>
Record fed-us-cong114-hr6501 · catalog fed-us-congress-bills-cong114 · updated 2026-11-15 by psicol fed-bills-cong114