# Veletri

NDC: 66215-403
Generic name: epoprostenol
Labeler / Manufacturer: Actelion Pharmaceuticals US, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20100422

FDA application: NDA022260

## Active ingredients

- EPOPROSTENOL: .5 mg/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"66215-403"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=66215-403
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=df502787-46ec-4dd1-a2c0-be90f6d95a5d