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NDC 64842-1020 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nametrifluridine and tipiracil
Labeler / ManufacturerTaiho Pharmaceutical Co., Ltd.
Marketing categoryNew Drug Application (innovator) · App NDA207981
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTIPIRACIL HYDROCHLORIDE (8.19 mg/1)
TRIFLURIDINE (20 mg/1)
Marketing started20150922
Package count3

External sources

Source: openFDA. Public-domain (CC0).