Zydus gets USFDA nod for Lamotrigine Extended-Release Tablets for seizures

Published On 2020-04-03 08:02 GMT   |   Update On 2020-04-03 08:02 GMT

Ahmedabad: Zydus Cadila has received final approval from the USFDA to market Lamotrigine Extended-Release Tablets USP in the strengths of 25 mg, 50 mg, 100 mg, 200 mg, 250 mg, and 300 mg.

This medication is indicated for the treatment of certain types of seizures and will be manufactured at the group's manufacturing facility at SEZ, Ahmedabad.

The group now has 283 approvals and has so far filed over 386 ANDAs since the commencement of the filing process in FY 2003-04.

Zydus Cadila is an innovative, global pharmaceutical company that discovers, develops, manufactures and markets a broad range of healthcare therapies.

The group employs nearly 25000 people worldwide and is dedicated to creating healthier communities globally. Zydus aspires to be a research-based pharmaceutical company by 2020.

Read also: Zydus gets USFDA tentative nod for Carbidopa, Levodopa Extended-Release Capsules



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