FdaApplication

ANDA 219538

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Identifiers

Properties

PropertyValue
applicant_nameAUROBINDO PHARMA LTD
application_typeANDA
approval_date2025-06-30

Products (1)

ProductActive ingredientStrengthDosage form
IBUPROFEN AND FAMOTIDINEFAMOTIDINE; IBUPROFEN26.6MG;800MGTABLET;ORAL

1 product