# nilotinib

NDC: 13668-711
Generic name: nilotinib
Labeler / Manufacturer: Torrent Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20251216

FDA application: ANDA218532

## Active ingredients

- NILOTINIB HYDROCHLORIDE MONOHYDRATE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"13668-711"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=13668-711
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b34e7fd4-53c5-46d8-bf8a-1fcbe7a16504