FDA NDC Directory · JSON-LD · Markdown

Iclusig

NDC 63020-536 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameponatinib hydrochloride
Labeler / ManufacturerTakeda Pharmaceuticals America, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA203469
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPONATINIB HYDROCHLORIDE (10 mg/1)
Marketing started20210111
Package count1

External sources

Source: openFDA. Public-domain (CC0).