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Zydus Cadila gets USFDA approval to market Mesalamine Delayed - Release Tablets USP, 1.2 g

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Capital Market
Last Updated : Jun 08 2017 | 12:01 AM IST

In US market

Zydus Cadila announced that USFDA has given its final approval to market Mesalamine Delayed - Release Tablets USP, 1.2 g in the US market. Zydus Cadila was the first to file an Abbreviated New Drug Application for a generic version of Lialda (mesalamine). The product will be manufactured at the Maurya manufacturing facility.

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First Published: Jun 07 2017 | 9:33 AM IST

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