FdaApplication

ANDA 200484

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Identifiers

Properties

PropertyValue
applicant_nameSUN PHARMACEUTICAL INDUSTRIES LTD
application_typeANDA
approval_date2014-04-23

Products (2)

ProductActive ingredientStrengthDosage form
NIACINNIACIN1GMTABLET, EXTENDED RELEASE;ORAL
NIACINNIACIN500MGTABLET, EXTENDED RELEASE;ORAL

2 products