FDA NDC Directory · JSON-LD · Markdown

Nilotinib

NDC 60505-3801 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic namenilotinib
Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA203640
Dosage form / routeCAPSULE · ORAL
Active ingredientsNILOTINIB (150 mg/1)
Marketing started20250523
Package count2

External sources

Source: openFDA. Public-domain (CC0).