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nilotinib

NDC 13668-711 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerTorrent Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA218532
Dosage form / routeCAPSULE · ORAL
Active ingredientsNILOTINIB HYDROCHLORIDE MONOHYDRATE (200 mg/1)
Marketing started20251216
Package count2

External sources

Source: openFDA. Public-domain (CC0).