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Glenmark Genercics Ltd, a subsidiary of the company, has received Abbreviated New Drug Application (ANDA) from the US Food and Drug Administration for the cream to market and distribute the product in the US market immediately, Glenmark Pharmaceuticals said in a filing to the Bombay Stock Exchange.
The product is targeted at a niche category in the dermatology segment and where competition is limited, the filing added.
The USFDA approval aligns with Glenmark's strategy to build on its established presence in the dermatology marketplace.


















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