# CLOFARABINE

NDC: 63323-572
Generic name: clofarabine
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20170510

FDA application: ANDA204029

## Active ingredients

- CLOFARABINE: 1 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-572"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-572
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fe6ff0f9-7610-4a69-9b75-da7ec4bb7744