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Spironolactone

NDC 0378-2146 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namespironolactone
Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040424
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSPIRONOLACTONE (25 mg/1)
Marketing started19810203
Package count2

External sources

Source: openFDA. Public-domain (CC0).