FdaApplication

NDA 018370

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Identifiers

Properties

PropertyValue
applicant_nameSUPERPHARM CORP
application_typeNDA
approval_date1983-02-10

Products (2)

ProductActive ingredientStrengthDosage form
FUROSEMIDEFUROSEMIDE20MGTABLET;ORAL
FUROSEMIDEFUROSEMIDE40MGTABLET;ORAL

2 products