Zydus receives USFDA final approval for Imatinib Mesylate Tablets

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Capital Market
Last Updated : Apr 09 2020 | 12:50 PM IST
Zydus Cadila has received final approval from the USFDA to market Imatinib Mesylate Tablets, 100 mg and 400 mg. (US RLD: Gleevec Tablets).

This medication is used to treat certain types of leukemia (blood cancer), bone marrow disorders, skin cancer and tumors of the stomach and digestive system. The drug will be manufactured at the group's formulation manufacturing facility at the SEZ, in Ahmedabad.

The group now has 285 approvals and has so far filed over 386 ANDAs since the commencement of the filing process in FY 2003-04.

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First Published: Apr 09 2020 | 12:34 PM IST

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