Amneal Pharmaceuticals Launching Mesalamine, Gets US FDA Approval for Lenalidomide

MT Newswires Live
19 Feb

Amneal Pharmaceuticals (AMRX) said Wednesday that it will launch mesalamine 800 milligram delayed-release tablets to treat moderately active ulcerative colitis in adults.

The company also said it has received approval from the US Food and Drug Administration for an abbreviated new drug application for lenalidomide capsules, which are used to treat blood cancers.

Amneal said that, in settlement of all product-related claims, Celgene has agreed to grant Amneal a license to Celgene's patents required to manufacture and sell generic lenalidomide in the US starting Jan. 31, 2026.

Amneal shares were up less than 1% in recent Wednesday premarket activity.

Price: 7.86, Change: +0.07, Percent Change: +0.9

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