FDA NDC Directory · JSON-LD · Markdown

LYTGOBI

NDC 64842-0120 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameFUTIBATINIB
Labeler / ManufacturerTAIHO PHARMACEUTICAL CO., LTD.
Marketing categoryNew Drug Application (innovator) · App NDA214801
Dosage form / routeTABLET · ORAL
Active ingredientsFUTIBATINIB (4 mg/1)
Marketing started20230203
Package count3

External sources

Source: openFDA. Public-domain (CC0).