FdaApplication

NDA 018369

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Identifiers

Properties

PropertyValue
applicant_nameWATSON LABORATORIES INC
application_typeNDA
approval_date1982-05-14

Products (2)

ProductActive ingredientStrengthDosage form
FUROSEMIDEFUROSEMIDE40MGTABLET;ORAL
FUROSEMIDEFUROSEMIDE20MGTABLET;ORAL

2 products