FDA NDC Directory · JSON-LD · Markdown

Bumex

NDC 30698-630 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameBumetanide
Labeler / ManufacturerValidus Pharmaceuticals LLC
Marketing categoryNew Drug Application (innovator) · App NDA018225
Dosage form / routeTABLET · ORAL
Active ingredientsBUMETANIDE (.5 mg/1)
Marketing started19830228
Package count1

External sources

Source: openFDA. Public-domain (CC0).