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Digoxin

NDC 57664-437 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076363
Dosage form / routeTABLET · ORAL
Active ingredientsDIGOXIN (125 ug/1)
Marketing started20150217
Package count2

External sources

Source: openFDA. Public-domain (CC0).