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Iclusig

NDC 63020-535 · 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 (15 mg/1)
Marketing started20121214
Package count2

External sources

Source: openFDA. Public-domain (CC0).