FdaApplication

ANDA 203285

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Identifiers

Properties

PropertyValue
applicant_nameZYDUS PHARMACEUTICALS USA INC
application_typeANDA
approval_date2025-04-28

Products (3)

ProductActive ingredientStrengthDosage form
NIACINNIACIN500MGTABLET, EXTENDED RELEASE;ORAL
NIACINNIACIN1GMTABLET, EXTENDED RELEASE;ORAL
NIACINNIACIN750MGTABLET, EXTENDED RELEASE;ORAL

3 products