Glenmark’s unit gets USFDA for Esomeprazole Magnesium delayed-release capsule

Madhu Balaji Updated - June 12, 2024 at 10:08 AM.

Glenmark Specialty SA of  Glenmark Pharmaceutical has received final approval from the United States Food & Drug Administration (USFDA) for Esomeprazole Magnesium delayed-release capsules USP, 20 mg (OTC).

The capsule will be distributed in the US by Glenmark Therapeutics Inc., USA. It is bioequivalent to Nexium 2 24 HR delayed-release capsules, 20 mg (OTC), of Haleon U.S. Holdings LLC.

Shares of Glenmark Pharmaceuticals traded at ₹1,188.90 on the NSE, down by 0.16 per cent as of 9.54 am.

Published on June 12, 2024 04:38

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