FDA NDC Directory · JSON-LD · Markdown

Spironolactone

NDC 72789-291 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040750
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsSPIRONOLACTONE (50 mg/1)
Marketing started20210104
Package count4

External sources

Source: openFDA. Public-domain (CC0).