FdaApplication

ANDA 091427

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Identifiers

Properties

PropertyValue
applicant_nameAUROBINDO PHARMA USA INC
application_typeANDA
approval_date2011-04-14

Products (1)

ProductActive ingredientStrengthDosage form
PAROXETINE HYDROCHLORIDEPAROXETINE HYDROCHLORIDEEQ 37.5MG BASETABLET, EXTENDED RELEASE;ORAL

1 product