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    <number>1683</number>
    <updateDate>2025-05-27T14:12:59Z</updateDate>
    <updateDateIncludingText>2025-05-27T14:12:59Z</updateDateIncludingText>
    <originChamber>House</originChamber>
    <originChamberCode>H</originChamberCode>
    <type>HR</type>
    <introducedDate>2023-03-21</introducedDate>
    <congress>118</congress>
    <cdata>
      <constitutionalAuthorityStatementText>&lt;pre&gt;[Congressional Record Volume 169, Number 51 (Tuesday, March 21, 2023)][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 Ms. MACE:H.R. 1683.Congress has the power to enact this legislation pursuantto the following:Article I, Section 8 of the U.S. ConstitutionThe single subject of this legislation is:Would expand consumer choices for FDA-approved genericanimal drugs for the care and treatment of both pets andlivestock.[Page H1302]&lt;/pre&gt;</constitutionalAuthorityStatementText>
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        <systemCode>hsif00</systemCode>
        <name>Energy and Commerce Committee</name>
        <chamber>House</chamber>
        <type>Standing</type>
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            <name>Health Subcommittee</name>
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                <name>Referred to</name>
                <date>2023-03-31T16:11:27Z</date>
              </item>
            </activities>
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        </subcommittees>
        <activities>
          <item>
            <name>Referred To</name>
            <date>2023-03-21T21:01:35Z</date>
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    <actions>
      <item>
        <actionDate>2023-03-31</actionDate>
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            <systemCode>hsif14</systemCode>
            <name>Health Subcommittee</name>
          </item>
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        <text>Referred to the Subcommittee on Health.</text>
        <type>Committee</type>
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      <item>
        <actionDate>2023-03-21</actionDate>
        <text>Referred to the House Committee on Energy and Commerce.</text>
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        <actionCode>H11100</actionCode>
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          <name>House floor actions</name>
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            <systemCode>hsif00</systemCode>
            <name>Energy and Commerce Committee</name>
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      <item>
        <actionDate>2023-03-21</actionDate>
        <text>Introduced in House</text>
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          <name>Library of Congress</name>
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        <actionDate>2023-03-21</actionDate>
        <text>Introduced in House</text>
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    <sponsors>
      <item>
        <bioguideId>M000194</bioguideId>
        <fullName>Rep. Mace, Nancy [R-SC-1]</fullName>
        <firstName>Nancy</firstName>
        <lastName>Mace</lastName>
        <party>R</party>
        <state>SC</state>
        <district>1</district>
        <isByRequest>N</isByRequest>
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    </sponsors>
    <policyArea>
      <name>Health</name>
    </policyArea>
    <subjects>
      <legislativeSubjects/>
      <policyArea>
        <name>Health</name>
        <updateDate>2023-04-06T13:45:24Z</updateDate>
      </policyArea>
    </subjects>
    <summaries>
      <summary>
        <versionCode>00</versionCode>
        <actionDate>2023-03-21</actionDate>
        <actionDesc>Introduced in House</actionDesc>
        <updateDate>2023-09-19T19:15:45Z</updateDate>
        <cdata>
          <text>&lt;p&gt;&lt;b&gt;Generic Animal Drug Advancement Act&lt;/b&gt;&lt;/p&gt; &lt;p&gt;This bill allows for the approval and corresponding labeling of generic animal drugs that are bioequivalent to another approved drug with respect to at least one species, rather than with respect to all of the same species. (Animal drugs are drugs that are intended for animals other than humans (e.g., pets and livestock). Animal drugs must be approved by the Food and Drug Administration before they may be offered on the commercial market.)&lt;/p&gt;</text>
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    </summaries>
    <title>Generic Animal Drug Advancement Act</title>
    <titles>
      <item>
        <titleType>Display Title</titleType>
        <titleTypeCode>45</titleTypeCode>
        <title>Generic Animal Drug Advancement Act</title>
        <updateDate>2024-07-24T15:23:16Z</updateDate>
      </item>
      <item>
        <titleType>Short Title(s) as Introduced</titleType>
        <titleTypeCode>101</titleTypeCode>
        <title>Generic Animal Drug Advancement Act</title>
        <updateDate>2024-05-24T13:41:34Z</updateDate>
        <billTextVersionName>Introduced in House</billTextVersionName>
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      </item>
      <item>
        <titleType>Official Title as Introduced</titleType>
        <titleTypeCode>6</titleTypeCode>
        <title>To amend the Federal Food, Drug, and Cosmetic Act to make certain changes with respect to the approval of abbreviated applications for the approval of new animal drugs, and for other purposes.</title>
        <updateDate>2024-03-18T20:29:13Z</updateDate>
        <billTextVersionName>Introduced in House</billTextVersionName>
        <billTextVersionCode>IH</billTextVersionCode>
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        <type>Introduced in House</type>
        <date>2023-03-21T04:00:00Z</date>
        <formats>
          <item>
            <url>https://www.govinfo.gov/content/pkg/BILLS-118hr1683ih/xml/BILLS-118hr1683ih.xml</url>
          </item>
        </formats>
      </item>
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    <latestAction>
      <actionDate>2023-03-31</actionDate>
      <text>Referred to the Subcommittee on Health.</text>
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    <dc:language>EN</dc:language>
    <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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