FDA NDC Directory · JSON-LD · Markdown

Furosemide

NDC 70518-4679 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA078010
Dosage form / routeTABLET · ORAL
Active ingredientsFUROSEMIDE (20 mg/1)
Marketing started20260622
Package count1

External sources

Source: openFDA. Public-domain (CC0).