# Nilotinib

NDC: 60505-3802
Generic name: nilotinib
Labeler / Manufacturer: Apotex Corp.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20250523

FDA application: ANDA203640

## Active ingredients

- NILOTINIB: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60505-3802"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60505-3802
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8283672c-619f-fe60-3d25-040f95ac1440