FDA NDC Directory · JSON-LD · Markdown

Bumetanide

NDC 0904-7016 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA209724
Dosage form / routeTABLET · ORAL
Active ingredientsBUMETANIDE (1 mg/1)
Marketing started20171018
Package count3

External sources

Source: openFDA. Public-domain (CC0).