FDA NDC Directory · JSON-LD · Markdown

SCEMBLIX

NDC 0078-1091 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameasciminib
Labeler / ManufacturerNovartis Pharmaceuticals Corporation
Marketing categoryNew Drug Application (innovator) · App NDA215358
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsASCIMINIB HYDROCHLORIDE (20 mg/1)
Marketing started20211029
Package count2

External sources

Source: openFDA. Public-domain (CC0).