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Digoxin

NDC 0904-5921 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA077002
Dosage form / routeTABLET · ORAL
Active ingredientsDIGOXIN (125 ug/1)
Marketing started20090610
Package count1

External sources

Source: openFDA. Public-domain (CC0).