FdaApplication

ANDA 203899

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Identifiers

Properties

PropertyValue
applicant_nameQUAGEN PHARMACEUTICALS LLC
application_typeANDA
approval_date2017-06-16

Products (2)

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

2 products