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Furosemide

NDC 51655-481 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryNew Drug Application (innovator) · App NDA018823
Dosage form / routeTABLET · ORAL
Active ingredientsFUROSEMIDE (20 mg/1)
Marketing started20201119
Package count2

External sources

Source: openFDA. Public-domain (CC0).