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INDIA'S LUPIN LTD GETS US FDA NOD FOR DIVALPROX EPILEPSY DRUG.
MUMBAI, Aug 1 Asia Pulse - Indian pharmaceutical firm Lupin Ltd (BSE:500257) on Thursday said it has received final approval from US Food and Drug Administrator for Divalprox Sodium Delayed Release tablets, used to control seizures in the treatment of epilepsy.
Lupin Pharmaceuticals Inc has received final approval for the company's abbreviated new drug application for Divalprox Sodium Delayed Release tablets in the strength of 125 mg, 250 mg and 500 mg, Lupin said in a filing to the Bombay Stock Exchange.
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Source: HighBeam Research, INDIA'S LUPIN LTD GETS US FDA NOD FOR DIVALPROX EPILEPSY DRUG.