FdaApplication

ANDA 213794

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Identifiers

Properties

PropertyValue
applicant_nameAUROBINDO PHARMA LTD
application_typeANDA
approval_date2020-05-08

Products (3)

ProductActive ingredientStrengthDosage form
IBUPROFENIBUPROFEN400MGTABLET;ORAL
IBUPROFENIBUPROFEN600MGTABLET;ORAL
IBUPROFENIBUPROFEN800MGTABLET;ORAL

3 products