FdaApplication

NDA 050687

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Identifiers

Properties

PropertyValue
applicant_nameSANKYO USA CORP
application_typeNDA
approval_date1992-08-07

Products (2)

ProductActive ingredientStrengthDosage form
BANANCEFPODOXIME PROXETILEQ 100MG BASETABLET;ORAL
BANANCEFPODOXIME PROXETILEQ 200MG BASETABLET;ORAL

2 products