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Furosemide

NDC 67046-0768 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077293
Dosage form / routeTABLET · ORAL
Active ingredientsFUROSEMIDE (20 mg/1)
Marketing started20260610
Package count1

External sources

Source: openFDA. Public-domain (CC0).