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Spironolactone

NDC 70518-3625 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA040750
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsSPIRONOLACTONE (25 mg/1)
Marketing started20230127
Package count4

External sources

Source: openFDA. Public-domain (CC0).