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    <constitutionalAuthorityStatementText><![CDATA[<pre>[Congressional Record Volume 166, Number 15 (Friday, January 24, 2020)][House]From the Congressional Record Online through the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]By Ms. MATSUI:H.R. 5668.Congress has the power to enact this legislation pursuantto the following:Article 1, Section 8 of the US Constitution[Page H537]</pre>]]></constitutionalAuthorityStatementText>
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        <title>Lower Health Care Costs Act</title>
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          <text>Referred to the Committee on Energy and Commerce, and in addition to the Committees on Ways and Means, Education and Labor, the Judiciary, Oversight and Reform, House Administration, Rules, the Budget, and Armed Services, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.</text>
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        <text>DEBATE - The House proceeded with forty minutes of debate on H.R. 5668.</text>
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        <fullName>Rep. Matsui, Doris O. [D-CA-6]</fullName>
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        <state>CA</state>
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        <fullName>Rep. Guthrie, Brett [R-KY-2]</fullName>
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        <state>KY</state>
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        <bioguideId>T000479</bioguideId>
        <fullName>Rep. Taylor, Van [R-TX-3]</fullName>
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        <district>3</district>
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        <pubDate>2020-10-29T20:08:00Z</pubDate>
        <title>H.R. 5668, Making Objective Drug Evidence Revisions for New Labeling  Act of 2020</title>
        <url>https://www.cbo.gov/publication/56712</url>
        <description>As ordered reported by the House Committee on Energy and Commerce on July 15, 2020</description>
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        <actionDate>2020-01-24</actionDate>
        <actionDesc>Introduced in House</actionDesc>
        <updateDate>2021-09-07T14:23:22Z</updateDate>
        <text><![CDATA[ <p><strong>Making Objective Drug Evidence Revisions for New Labeling Act of 2020 or the MODERN Labeling Act of 2020</strong></p> <p>This bill authorizes the Food and Drug Administration (FDA) to require updates to outdated labels for certain generic drugs if the updates will provide a public health benefit. Generally, the FDA may use this authority to update the label of a generic version of a brand-name drug that has been withdrawn from the market for reasons other than safety or effectiveness.</p>]]></text>
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        <actionDate>2020-11-17</actionDate>
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        <updateDate>2021-09-07T15:13:18Z</updateDate>
        <text><![CDATA[ <p><strong>Making Objective Drug Evidence Revisions for New Labeling Act of 2020 or the MODERN Labeling Act of 2020</strong></p> <p>This bill authorizes the Food and Drug Administration (FDA) to require updates to outdated labels for certain generic drugs if the updates will provide a public health benefit. Generally, the FDA may use this authority to update the label of a generic version of a brand-name drug that has been withdrawn from the market for reasons other than safety or effectiveness.</p>]]></text>
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    <title>MODERN Labeling Act of 2020</title>
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        <title>To amend the Federal Food, Drug, and Cosmetic Act to modernize the labeling of certain generic drugs, and for other purposes.</title>
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