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SPIRONOLACTONE

NDC 76420-558 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA089424
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSPIRONOLACTONE (100 mg/1)
Marketing started19860723
Package count4

External sources

Source: openFDA. Public-domain (CC0).