# BOSULIF

NDC: 63539-193
Generic name: Bosutinib
Labeler / Manufacturer: U.S. Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120904

FDA application: NDA203341

## Active ingredients

- BOSUTINIB MONOHYDRATE: 400 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63539-193"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63539-193
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d5929f91-6496-4c0e-97e8-0bd524e15763