FDA NDC Directory · JSON-LD · Markdown

Digoxin

NDC 60687-858 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA215307
Dosage form / routeTABLET · ORAL
Active ingredientsDIGOXIN (.125 mg/1)
Marketing started20250206
Package count1

External sources

Source: openFDA. Public-domain (CC0).