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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/Press+Releases/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
&lt;div id=&quot;prni_dvprnejpgbc87left&quot; dir=&quot;ltr&quot; style=&quot;width: 100%; text-align: left;&quot;&gt;&lt;img id=&quot;prnejpgbc87left&quot; style=&quot;width: 331px; height: 400px;&quot; title=&quot;Lupin Logo&quot; src=&quot;https://mma.prnewswire.com/media/2461104/Lupin_Logo.jpg&quot; alt=&quot;Lupin Logo&quot; align=&quot;middle&quot; /&gt;&lt;/div&gt;&lt;p&gt;Eribulin Mesylate Injection, 1</description>
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   <pubDate>Wed, 03 Jun 2026 03:11:00 -0400</pubDate>
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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/Press+Releases/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
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   <pubDate>Wed, 03 Jun 2026 03:11:00 -0400</pubDate>
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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/Press+Releases/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/Press+Releases/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/Press+Releases/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/Press+Releases/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/Press+Releases/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/Press+Releases/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
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   <pubDate>Wed, 03 Jun 2026 03:11:00 -0400</pubDate>
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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/Press+Releases/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/Press+Releases/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/PRNewswire/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/PRNewswire/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/PRNewswire/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
&lt;div id=&quot;prni_dvprnejpgbc87left&quot; dir=&quot;ltr&quot; style=&quot;width: 100%; text-align: left;&quot;&gt;&lt;img id=&quot;prnejpgbc87left&quot; style=&quot;width: 331px; height: 400px;&quot; title=&quot;Lupin Logo&quot; src=&quot;https://mma.prnewswire.com/media/2461104/Lupin_Logo.jpg&quot; alt=&quot;Lupin Logo&quot; align=&quot;middle&quot; /&gt;&lt;/div&gt;&lt;p&gt;Eribulin Mesylate Injection, 1</description>
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   <pubDate>Wed, 03 Jun 2026 03:11:00 -0400</pubDate>
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   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/PRNewswire/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
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  <item>
   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/PRNewswire/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
&lt;div id=&quot;prni_dvprnejpgbc87left&quot; dir=&quot;ltr&quot; style=&quot;width: 100%; text-align: left;&quot;&gt;&lt;img id=&quot;prnejpgbc87left&quot; style=&quot;width: 331px; height: 400px;&quot; title=&quot;Lupin Logo&quot; src=&quot;https://mma.prnewswire.com/media/2461104/Lupin_Logo.jpg&quot; alt=&quot;Lupin Logo&quot; align=&quot;middle&quot; /&gt;&lt;/div&gt;&lt;p&gt;Eribulin Mesylate Injection, 1</description>
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   <pubDate>Wed, 03 Jun 2026 03:11:00 -0400</pubDate>
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  <item>
   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/PRNewswire/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
&lt;div id=&quot;prni_dvprnejpgbc87left&quot; dir=&quot;ltr&quot; style=&quot;width: 100%; text-align: left;&quot;&gt;&lt;img id=&quot;prnejpgbc87left&quot; style=&quot;width: 331px; height: 400px;&quot; title=&quot;Lupin Logo&quot; src=&quot;https://mma.prnewswire.com/media/2461104/Lupin_Logo.jpg&quot; alt=&quot;Lupin Logo&quot; align=&quot;middle&quot; /&gt;&lt;/div&gt;&lt;p&gt;Eribulin Mesylate Injection, 1</description>
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   <pubDate>Wed, 03 Jun 2026 03:11:00 -0400</pubDate>
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  <item>
   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/PRNewswire/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
&lt;div id=&quot;prni_dvprnejpgbc87left&quot; dir=&quot;ltr&quot; style=&quot;width: 100%; text-align: left;&quot;&gt;&lt;img id=&quot;prnejpgbc87left&quot; style=&quot;width: 331px; height: 400px;&quot; title=&quot;Lupin Logo&quot; src=&quot;https://mma.prnewswire.com/media/2461104/Lupin_Logo.jpg&quot; alt=&quot;Lupin Logo&quot; align=&quot;middle&quot; /&gt;&lt;/div&gt;&lt;p&gt;Eribulin Mesylate Injection, 1</description>
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   <pubDate>Wed, 03 Jun 2026 03:11:00 -0400</pubDate>
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  <item>
   <title>Lupin and Natco Receive Approval from U.S. FDA for Eribulin Mesylate Injection</title>
   <link>http://www.streetinsider.com/PRNewswire/Lupin+and+Natco+Receive+Approval+from+U.S.+FDA+for+Eribulin+Mesylate+Injection/26594306.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/in..bombay&quot; idsrc=&quot;xmltag.org&quot; &gt;MUMBAI, India&lt;/location&gt; and &lt;location value=&quot;LU/us.fl.naples&quot; idsrc=&quot;xmltag.org&quot; &gt;NAPLES, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 3, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Global pharma major &lt;span value=&quot;Bombay:500257&quot; idsrc=&quot;xmltag.org&quot; &gt;Lupin Limited&lt;/span&gt; (Lupin) (BSE: 500257) (NSE: LUPIN) (REUTERS: LUPIN.BO) (BLOOMBERG: LPCIN) and its alliance partner Natco Pharma Limited (Natco) today announced the approval from the &lt;span&gt;United States Food and Drug Administration&lt;/span&gt; (&lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. FDA) for Natco's Abbreviated New Drug Application (ANDA) for Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials.&lt;/p&gt;
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   <pubDate>Wed, 03 Jun 2026 03:11:00 -0400</pubDate>
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  <item>
   <title>Lupin presents phase 1 data for cancer drug LNP8701 at ASCO meeting</title>
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&lt;p&gt;Lupin Limited (BSE: 500257, NSE: LUPIN) announced that results from its Phase 1a trial of LNP8701, an experimental cancer treatment, have been presented at the American Society of Clinical Oncology Annual Meeting held May 29-June 2, 2026, in Chicago.&lt;/p&gt;

&lt;p&gt;The study evaluated LNP8701, an orally administered SOS1 inhibitor designed to block oncogenic signaling that promotes tumor growth, in patients with metastatic solid tumors. According to the company's statement, the drug demonstrated tolerability and safety across all tested dosing levels.&lt;/p&gt;

&lt;p&gt;The abstract, published in the Developmental Therapeutics track, reported that two patients completed 12 cycles of LNP8701 monotherapy and one patient completed 14</description>
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   <pubDate>Thu, 28 May 2026 08:26:21 -0400</pubDate>
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   <title>Lupin presents phase 1 data for cancer drug LNP8701 at ASCO meeting</title>
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&lt;p&gt;Lupin Limited (BSE: 500257, NSE: LUPIN) announced that results from its Phase 1a trial of LNP8701, an experimental cancer treatment, have been presented at the American Society of Clinical Oncology Annual Meeting held May 29-June 2, 2026, in Chicago.&lt;/p&gt;

&lt;p&gt;The study evaluated LNP8701, an orally administered SOS1 inhibitor designed to block oncogenic signaling that promotes tumor growth, in patients with metastatic solid tumors. According to the company's statement, the drug demonstrated tolerability and safety across all tested dosing levels.&lt;/p&gt;

&lt;p&gt;The abstract, published in the Developmental Therapeutics track, reported that two patients completed 12 cycles of LNP8701 monotherapy and one patient completed 14</description>
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   <pubDate>Thu, 28 May 2026 08:26:21 -0400</pubDate>
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   <title>Lupin presents phase 1 data for cancer drug LNP8701 at ASCO meeting</title>
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&lt;p&gt;Lupin Limited (BSE: 500257, NSE: LUPIN) announced that results from its Phase 1a trial of LNP8701, an experimental cancer treatment, have been presented at the American Society of Clinical Oncology Annual Meeting held May 29-June 2, 2026, in Chicago.&lt;/p&gt;

&lt;p&gt;The study evaluated LNP8701, an orally administered SOS1 inhibitor designed to block oncogenic signaling that promotes tumor growth, in patients with metastatic solid tumors. According to the company's statement, the drug demonstrated tolerability and safety across all tested dosing levels.&lt;/p&gt;

&lt;p&gt;The abstract, published in the Developmental Therapeutics track, reported that two patients completed 12 cycles of LNP8701 monotherapy and one patient completed 14</description>
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   <title>Lupin presents phase 1 data for cancer drug LNP8701 at ASCO meeting</title>
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&lt;p&gt;Lupin Limited (BSE: 500257, NSE: LUPIN) announced that results from its Phase 1a trial of LNP8701, an experimental cancer treatment, have been presented at the American Society of Clinical Oncology Annual Meeting held May 29-June 2, 2026, in Chicago.&lt;/p&gt;

&lt;p&gt;The study evaluated LNP8701, an orally administered SOS1 inhibitor designed to block oncogenic signaling that promotes tumor growth, in patients with metastatic solid tumors. According to the company's statement, the drug demonstrated tolerability and safety across all tested dosing levels.&lt;/p&gt;

&lt;p&gt;The abstract, published in the Developmental Therapeutics track, reported that two patients completed 12 cycles of LNP8701 monotherapy and one patient completed 14</description>
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   <title>Lupin presents phase 1 data for cancer drug LNP8701 at ASCO meeting</title>
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   <description>

&lt;p&gt;Lupin Limited (BSE: 500257, NSE: LUPIN) announced that results from its Phase 1a trial of LNP8701, an experimental cancer treatment, have been presented at the American Society of Clinical Oncology Annual Meeting held May 29-June 2, 2026, in Chicago.&lt;/p&gt;

&lt;p&gt;The study evaluated LNP8701, an orally administered SOS1 inhibitor designed to block oncogenic signaling that promotes tumor growth, in patients with metastatic solid tumors. According to the company's statement, the drug demonstrated tolerability and safety across all tested dosing levels.&lt;/p&gt;

&lt;p&gt;The abstract, published in the Developmental Therapeutics track, reported that two patients completed 12 cycles of LNP8701 monotherapy and one patient completed 14</description>
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