FdaApplication

NDA 216993

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Identifiers

Properties

PropertyValue
applicant_nameDAIICHI SANKYO INC
application_typeNDA
approval_date2023-07-20

Products (2)

ProductActive ingredientStrengthDosage form
VANFLYTAQUIZARTINIB DIHYDROCHLORIDEEQ 26.5MG BASETABLET;ORAL
VANFLYTAQUIZARTINIB DIHYDROCHLORIDEEQ 17.7MG BASETABLET;ORAL

2 products