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Zydus Cadila gets USFDA final approval for Acetazolamide

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has received the final approval from the USFI)A to market for Injection USP (US RLD Diamox for Injection), 500 mg per single-dose vial.

It will be manufactured at the group's formulations manufacturing facility at Moraiya,

is a potent carbonic anhydrase inhibitor, effective in the control of fluid secretion (e.g. some types of glaucoma), (e. g. epilepsy) and promotion of diuresis in instances of abnormal fluid retention (e.g. cardiac edema).

The group now has 262 approvals and has so far filed over 350 ANDAs since the commencement of the filing process in FY 2003-04.

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(This story has not been edited by Business Standard staff and is auto-generated from a syndicated feed.)

First Published: Wed, April 17 2019. 18:51 IST
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