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Spironolactone

NDC 82804-976 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA040750
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsSPIRONOLACTONE (50 mg/1)
Marketing started20210104
Package count7

External sources

Source: openFDA. Public-domain (CC0).