FDA NDC Directory · JSON-LD · Markdown

LAMPIT

NDC 50419-751 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namenifurtimox
Labeler / ManufacturerBayer HealthCare Pharmaceuticals Inc.
Marketing categoryNew Drug Application (innovator) · App NDA213464
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNIFURTIMOX (120 mg/1)
Marketing started20201001
Package count1

External sources

Source: openFDA. Public-domain (CC0).