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Bumetanide

NDC 72888-021 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAdvagen Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA213942
Dosage form / routeTABLET · ORAL
Active ingredientsBUMETANIDE (2 mg/1)
Marketing started20250116
Package count1

External sources

Source: openFDA. Public-domain (CC0).