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Spironolactone

NDC 54348-340 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameSPIRONOLACTONE
Labeler / ManufacturerPharmPak, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091426
Dosage form / routeTABLET · ORAL
Active ingredientsSPIRONOLACTONE (50 mg/1)
Marketing started20190709
Package count1

External sources

Source: openFDA. Public-domain (CC0).