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Spironolactone

NDC 65162-511 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA091426
Dosage form / routeTABLET · ORAL
Active ingredientsSPIRONOLACTONE (25 mg/1)
Marketing started20100802
Package count7

External sources

Source: openFDA. Public-domain (CC0).