FDA NDC Directory · JSON-LD · Markdown

FUROSEMIDE

NDC 51655-269 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namefurosemide
Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077293
Dosage form / routeTABLET · ORAL
Active ingredientsFUROSEMIDE (20 mg/1)
Marketing started20220808
Package count4

External sources

Source: openFDA. Public-domain (CC0).