FDA NDC Directory · JSON-LD · Markdown

Bumetanide

NDC 76282-797 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerExelan Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212931
Dosage form / routeTABLET · ORAL
Active ingredientsBUMETANIDE (.5 mg/1)
Marketing started20250301
Package count1

External sources

Source: openFDA. Public-domain (CC0).