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    <introducedDate>2025-03-05</introducedDate>
    <congress>119</congress>
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      <constitutionalAuthorityStatementText>&lt;pre&gt;[Congressional Record Volume 171, Number 42 (Wednesday, March 5, 2025)][House]From the Congressional Record Online through the Government Publishing Office [&lt;a href="https://www.gpo.gov"&gt;www.gpo.gov&lt;/a&gt;]By Mr. DUNN of Florida:H.R. 1843.Congress has the power to enact this legislation pursuantto the following:Clause 3 of Section 8 of Article I of the Constitution[Page H1009]&lt;/pre&gt;</constitutionalAuthorityStatementText>
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        <title>Consolidated Appropriations Act, 2026</title>
        <congress>119</congress>
        <number>7148</number>
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          <actionDate>2026-02-03</actionDate>
          <text>Became Public Law No: 119-75.</text>
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        <congress>119</congress>
        <number>891</number>
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        <latestAction>
          <actionDate>2025-03-06</actionDate>
          <text>Read twice and referred to the Committee on Finance.</text>
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        <title>Increasing Transparency in Generic Drug Applications Act</title>
        <congress>119</congress>
        <number>1302</number>
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          <actionDate>2025-04-03</actionDate>
          <text>Read twice and referred to the Committee on Health, Education, Labor, and Pensions.</text>
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        <title>Lower Costs for Everyday Americans Act</title>
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        <number>1768</number>
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          <actionDate>2025-03-03</actionDate>
          <text>Referred to the Committee on Energy and Commerce, and in addition to the Committees on Ways and Means, the Budget, the Judiciary, and Education and Workforce, 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>Referred to the House Committee on Energy and Commerce.</text>
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        <bioguideId>D000628</bioguideId>
        <fullName>Rep. Dunn, Neal P. [R-FL-2]</fullName>
        <firstName>Neal</firstName>
        <lastName>Dunn</lastName>
        <party>R</party>
        <state>FL</state>
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        <district>2</district>
        <isByRequest>N</isByRequest>
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    <cosponsors>
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        <bioguideId>M001225</bioguideId>
        <fullName>Rep. Mullin, Kevin [D-CA-15]</fullName>
        <firstName>Kevin</firstName>
        <lastName>Mullin</lastName>
        <party>D</party>
        <state>CA</state>
        <district>15</district>
        <sponsorshipDate>2025-03-05</sponsorshipDate>
        <isOriginalCosponsor>True</isOriginalCosponsor>
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    <policyArea>
      <name>Health</name>
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      <policyArea>
        <name>Health</name>
        <updateDate>2025-03-21T17:32:00Z</updateDate>
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        <actionDesc>Introduced in House</actionDesc>
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          <text>&lt;p&gt;This bill requires the Food and Drug Administration (FDA) to inform generic drug applicants, upon request or during review, whether the drug is qualitatively and quantitatively the same as the listed brand-name drug (and if not, the reasons why). The FDA must also update or publish guidance on how it makes such determinations.&lt;/p&gt;</text>
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    <title>To amend the Federal Food, Drug, and Cosmetic Act to increase transparency in generic drug applications.</title>
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        <titleType>Official Title as Introduced</titleType>
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        <title>To amend the Federal Food, Drug, and Cosmetic Act to increase transparency in generic drug applications.</title>
        <updateDate>2025-03-21T04:04:34Z</updateDate>
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        <title>To amend the Federal Food, Drug, and Cosmetic Act to increase transparency in generic drug applications.</title>
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    <latestAction>
      <actionDate>2025-03-05</actionDate>
      <text>Referred to the House Committee on Energy and Commerce.</text>
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    <dc:rights>Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain.</dc:rights>
    <dc:contributor>Congressional Research Service, Library of Congress</dc:contributor>
    <dc:description>This file contains bill summaries and statuses for federal legislation. A bill summary describes the most significant provisions of a piece of legislation and details the effects the legislative text may have on current law and federal programs. Bill summaries are authored by the Congressional Research Service (CRS) of the Library of Congress. As stated in Public Law 91-510 (2 USC 166 (d)(6)), one of the duties of CRS is "to prepare summaries and digests of bills and resolutions of a public general nature introduced in the Senate or House of Representatives". For more information, refer to the User Guide that accompanies this file.</dc:description>
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