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   <title>FDA approves rituximab biosimilar for Fresenius Kabi's U.S. portfolio</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</link>
   <description>

&lt;p&gt;Fresenius Kabi, an operating company of Fresenius SE &amp; Co. KGaA (Frankfurt/Xetra: FRE), announced that the U.S. Food and Drug Administration has approved a rituximab biosimilar developed and manufactured by Dr. Reddy's Laboratories, referencing Rituxan® (rituximab).&lt;/p&gt;

&lt;p&gt;Under an exclusive commercialization agreement, Fresenius Kabi holds the rights to market the biosimilar in the United States, while Dr. Reddy's Laboratories developed, manufactured, and submitted the product for approval.&lt;/p&gt;

&lt;p&gt;Rituximab is a monoclonal antibody that targets the CD20 antigen on B lymphocytes. It is used in the treatment of adults with non-Hodgkin lymphoma, chronic lymphocytic leukemia, rheumatoid arthritis, granulomatosis with polyangiitis, and microscopic polyangiitis.&lt;/p&gt;

&lt;p&gt;The FDA</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</guid>
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   <title>FDA approves rituximab biosimilar for Fresenius Kabi's U.S. portfolio</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</link>
   <description>

&lt;p&gt;Fresenius Kabi, an operating company of Fresenius SE &amp; Co. KGaA (Frankfurt/Xetra: FRE), announced that the U.S. Food and Drug Administration has approved a rituximab biosimilar developed and manufactured by Dr. Reddy's Laboratories, referencing Rituxan® (rituximab).&lt;/p&gt;

&lt;p&gt;Under an exclusive commercialization agreement, Fresenius Kabi holds the rights to market the biosimilar in the United States, while Dr. Reddy's Laboratories developed, manufactured, and submitted the product for approval.&lt;/p&gt;

&lt;p&gt;Rituximab is a monoclonal antibody that targets the CD20 antigen on B lymphocytes. It is used in the treatment of adults with non-Hodgkin lymphoma, chronic lymphocytic leukemia, rheumatoid arthritis, granulomatosis with polyangiitis, and microscopic polyangiitis.&lt;/p&gt;

&lt;p&gt;The FDA</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</guid>
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   <title>FDA approves rituximab biosimilar for Fresenius Kabi's U.S. portfolio</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</link>
   <description>

&lt;p&gt;Fresenius Kabi, an operating company of Fresenius SE &amp; Co. KGaA (Frankfurt/Xetra: FRE), announced that the U.S. Food and Drug Administration has approved a rituximab biosimilar developed and manufactured by Dr. Reddy's Laboratories, referencing Rituxan® (rituximab).&lt;/p&gt;

&lt;p&gt;Under an exclusive commercialization agreement, Fresenius Kabi holds the rights to market the biosimilar in the United States, while Dr. Reddy's Laboratories developed, manufactured, and submitted the product for approval.&lt;/p&gt;

&lt;p&gt;Rituximab is a monoclonal antibody that targets the CD20 antigen on B lymphocytes. It is used in the treatment of adults with non-Hodgkin lymphoma, chronic lymphocytic leukemia, rheumatoid arthritis, granulomatosis with polyangiitis, and microscopic polyangiitis.&lt;/p&gt;

&lt;p&gt;The FDA</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</guid>
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   <title>FDA approves rituximab biosimilar for Fresenius Kabi's U.S. portfolio</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</link>
   <description>

&lt;p&gt;Fresenius Kabi, an operating company of Fresenius SE &amp; Co. KGaA (Frankfurt/Xetra: FRE), announced that the U.S. Food and Drug Administration has approved a rituximab biosimilar developed and manufactured by Dr. Reddy's Laboratories, referencing Rituxan® (rituximab).&lt;/p&gt;

&lt;p&gt;Under an exclusive commercialization agreement, Fresenius Kabi holds the rights to market the biosimilar in the United States, while Dr. Reddy's Laboratories developed, manufactured, and submitted the product for approval.&lt;/p&gt;

&lt;p&gt;Rituximab is a monoclonal antibody that targets the CD20 antigen on B lymphocytes. It is used in the treatment of adults with non-Hodgkin lymphoma, chronic lymphocytic leukemia, rheumatoid arthritis, granulomatosis with polyangiitis, and microscopic polyangiitis.&lt;/p&gt;

&lt;p&gt;The FDA</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</guid>
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   <title>FDA approves rituximab biosimilar for Fresenius Kabi's U.S. portfolio</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</link>
   <description>

&lt;p&gt;Fresenius Kabi, an operating company of Fresenius SE &amp; Co. KGaA (Frankfurt/Xetra: FRE), announced that the U.S. Food and Drug Administration has approved a rituximab biosimilar developed and manufactured by Dr. Reddy's Laboratories, referencing Rituxan® (rituximab).&lt;/p&gt;

&lt;p&gt;Under an exclusive commercialization agreement, Fresenius Kabi holds the rights to market the biosimilar in the United States, while Dr. Reddy's Laboratories developed, manufactured, and submitted the product for approval.&lt;/p&gt;

&lt;p&gt;Rituximab is a monoclonal antibody that targets the CD20 antigen on B lymphocytes. It is used in the treatment of adults with non-Hodgkin lymphoma, chronic lymphocytic leukemia, rheumatoid arthritis, granulomatosis with polyangiitis, and microscopic polyangiitis.&lt;/p&gt;

&lt;p&gt;The FDA</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</guid>
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   <title>FDA approves rituximab biosimilar for Fresenius Kabi's U.S. portfolio</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</link>
   <description>

&lt;p&gt;Fresenius Kabi, an operating company of Fresenius SE &amp; Co. KGaA (Frankfurt/Xetra: FRE), announced that the U.S. Food and Drug Administration has approved a rituximab biosimilar developed and manufactured by Dr. Reddy's Laboratories, referencing Rituxan® (rituximab).&lt;/p&gt;

&lt;p&gt;Under an exclusive commercialization agreement, Fresenius Kabi holds the rights to market the biosimilar in the United States, while Dr. Reddy's Laboratories developed, manufactured, and submitted the product for approval.&lt;/p&gt;

&lt;p&gt;Rituximab is a monoclonal antibody that targets the CD20 antigen on B lymphocytes. It is used in the treatment of adults with non-Hodgkin lymphoma, chronic lymphocytic leukemia, rheumatoid arthritis, granulomatosis with polyangiitis, and microscopic polyangiitis.&lt;/p&gt;

&lt;p&gt;The FDA</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</guid>
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  <item>
   <title>FDA approves rituximab biosimilar for Fresenius Kabi's U.S. portfolio</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</link>
   <description>

&lt;p&gt;Fresenius Kabi, an operating company of Fresenius SE &amp; Co. KGaA (Frankfurt/Xetra: FRE), announced that the U.S. Food and Drug Administration has approved a rituximab biosimilar developed and manufactured by Dr. Reddy's Laboratories, referencing Rituxan® (rituximab).&lt;/p&gt;

&lt;p&gt;Under an exclusive commercialization agreement, Fresenius Kabi holds the rights to market the biosimilar in the United States, while Dr. Reddy's Laboratories developed, manufactured, and submitted the product for approval.&lt;/p&gt;

&lt;p&gt;Rituximab is a monoclonal antibody that targets the CD20 antigen on B lymphocytes. It is used in the treatment of adults with non-Hodgkin lymphoma, chronic lymphocytic leukemia, rheumatoid arthritis, granulomatosis with polyangiitis, and microscopic polyangiitis.&lt;/p&gt;

&lt;p&gt;The FDA</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</guid>
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   <title>FDA approves rituximab biosimilar for Fresenius Kabi's U.S. portfolio</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</link>
   <description>

&lt;p&gt;Fresenius Kabi, an operating company of Fresenius SE &amp; Co. KGaA (Frankfurt/Xetra: FRE), announced that the U.S. Food and Drug Administration has approved a rituximab biosimilar developed and manufactured by Dr. Reddy's Laboratories, referencing Rituxan® (rituximab).&lt;/p&gt;

&lt;p&gt;Under an exclusive commercialization agreement, Fresenius Kabi holds the rights to market the biosimilar in the United States, while Dr. Reddy's Laboratories developed, manufactured, and submitted the product for approval.&lt;/p&gt;

&lt;p&gt;Rituximab is a monoclonal antibody that targets the CD20 antigen on B lymphocytes. It is used in the treatment of adults with non-Hodgkin lymphoma, chronic lymphocytic leukemia, rheumatoid arthritis, granulomatosis with polyangiitis, and microscopic polyangiitis.&lt;/p&gt;

&lt;p&gt;The FDA</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</guid>
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  <item>
   <title>FDA approves rituximab biosimilar for Fresenius Kabi's U.S. portfolio</title>
   <link>http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</link>
   <description>

&lt;p&gt;Fresenius Kabi, an operating company of Fresenius SE &amp; Co. KGaA (Frankfurt/Xetra: FRE), announced that the U.S. Food and Drug Administration has approved a rituximab biosimilar developed and manufactured by Dr. Reddy's Laboratories, referencing Rituxan® (rituximab).&lt;/p&gt;

&lt;p&gt;Under an exclusive commercialization agreement, Fresenius Kabi holds the rights to market the biosimilar in the United States, while Dr. Reddy's Laboratories developed, manufactured, and submitted the product for approval.&lt;/p&gt;

&lt;p&gt;Rituximab is a monoclonal antibody that targets the CD20 antigen on B lymphocytes. It is used in the treatment of adults with non-Hodgkin lymphoma, chronic lymphocytic leukemia, rheumatoid arthritis, granulomatosis with polyangiitis, and microscopic polyangiitis.&lt;/p&gt;

&lt;p&gt;The FDA</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/FDA+approves+rituximab+biosimilar+for+Fresenius+Kabi%27s+U.S.+portfolio/26857858.html</guid>
   <pubDate>Mon, 03 Aug 2026 16:09:13 -0400</pubDate>
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   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</guid>
   <pubDate>Mon, 03 Aug 2026 16:09:00 -0400</pubDate>
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   	  </item>
  <item>
   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</guid>
   <pubDate>Mon, 03 Aug 2026 16:09:00 -0400</pubDate>
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  <item>
   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</guid>
   <pubDate>Mon, 03 Aug 2026 16:09:00 -0400</pubDate>
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  <item>
   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</guid>
   <pubDate>Mon, 03 Aug 2026 16:09:00 -0400</pubDate>
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  <item>
   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</guid>
   <pubDate>Mon, 03 Aug 2026 16:09:00 -0400</pubDate>
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  <item>
   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</guid>
   <pubDate>Mon, 03 Aug 2026 16:09:00 -0400</pubDate>
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  <item>
   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</guid>
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  <item>
   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</guid>
   <pubDate>Mon, 03 Aug 2026 16:09:00 -0400</pubDate>
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  <item>
   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</guid>
   <pubDate>Mon, 03 Aug 2026 16:09:00 -0400</pubDate>
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  <item>
   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Business+Wire/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</guid>
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  <item>
   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Business+Wire/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</guid>
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  <item>
   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Business+Wire/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
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   <pubDate>Mon, 03 Aug 2026 16:09:00 -0400</pubDate>
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   	  </item>
  <item>
   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Business+Wire/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</guid>
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   	  </item>
  <item>
   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Business+Wire/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</guid>
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   	  </item>
  <item>
   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Business+Wire/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</guid>
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  <item>
   <title>Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market</title>
   <link>http://www.streetinsider.com/Business+Wire/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;b&gt;U.S. FDA approves rituximab biosimilar candidate developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan® (rituximab)&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Rituximab is a CD20-directed cytolytic antibody used across multiple oncology and immunology indications&lt;/b&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;b&gt;Approval expands Fresenius Kabi's U.S. biosimilars portfolio and reinforces its commitment to improving access to biologic medicines in the U.S. market&lt;/b&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    BAD HOMBURG, Germany--(BUSINESS WIRE)--
Fresenius Kabi, an operating company of Fresenius, announced today that the U.S. Food and Drug Administration (FDA) has approved a rituximab biosimilar developed by Dr. Reddy's Laboratories (DRL), a biosimilar to Rituxan®* (rituximab).1

&lt;/p&gt;&lt;p&gt;
Under an exclusive commercialization agreement, Fresenius Kabi holds exclusive rights to commercialize</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Fresenius+Announces+FDA+Approval+of+Rituximab+Biosimilar+for+the+U.S.+Market/26857850.html</guid>
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