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Lupin receives USFDA approval for Meclizine Hydrochloride Tablets

14 Aug 2022 , 01:31 AM

Lupin today announced that it has received approval from the United States Food and Drug Administration FDA for its Abbreviated New Drug Application ANDA Meclizine Hydrochloride Tablets USP 125 mg 25 mg and 50 mg to market a generic equivalent of Antivert Tablets 125 mg 25 mg and 50 mg of Casper Pharma LLC The product will be manufactured at Lupins facility in Goa India Meclizine Hydrochloride Tablets RLD Antivert had estimated annual sales of USD 29 million in the US IQVIA MAT June 2022

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