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Digoxin

NDC 82804-244 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA076268
Dosage form / routeTABLET · ORAL
Active ingredientsDIGOXIN (250 ug/1)
Marketing started20220901
Package count1

External sources

Source: openFDA. Public-domain (CC0).