FdaApplication

NDA 050688

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Identifiers

Properties

PropertyValue
applicant_nameSANKYO USA CORP
application_typeNDA
approval_date1992-08-07

Products (2)

ProductActive ingredientStrengthDosage form
BANANCEFPODOXIME PROXETILEQ 50MG BASE/5MLFOR SUSPENSION;ORAL
BANANCEFPODOXIME PROXETILEQ 100MG BASE/5MLFOR SUSPENSION;ORAL

2 products