# BUSULFEX

NDC: 59148-070
Generic name: busulfan
Labeler / Manufacturer: Otsuka America Pharmaceutical, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 19990204

FDA application: NDA020954

## Active ingredients

- BUSULFAN: 6 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59148-070"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59148-070
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5cb9d285-1803-4a99-946a-d0b239b32df6