# DEFITELIO

NDC: 68727-800
Generic name: defibrotide sodium
Labeler / Manufacturer: Jazz Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20160330

FDA application: NDA208114

## Active ingredients

- DEFIBROTIDE SODIUM: 80 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68727-800"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68727-800
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2c3db989-d7ad-41ed-9ebf-698dcf6c24ec