FDA NDC Directory · JSON-LD · Markdown

FUROSCIX

NDC 71767-111 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic namefurosemide
Labeler / ManufacturerscPharmaceuticals Inc., a wholly owned subsidiary of MannKind Corporation
Marketing categoryNew Drug Application (innovator) · App NDA209988
Dosage form / routeINJECTION · SUBCUTANEOUS
Active ingredientsFUROSEMIDE (80 mg/mL)
Marketing started20260727
Package count1

External sources

Source: openFDA. Public-domain (CC0).