United States · FDA National Drug Code directory
Veletri
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 66215-403_39e8b7f8-f82a-4083-a284-ce571a87ce97
- Product NDC
- 66215-403
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- epoprostenol
- Labeler
- Actelion Pharmaceuticals US, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20100422
- Source listing expiry
- 20261231
Source-listed ingredients
- EPOPROSTENOL — .5 mg/10mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 CARTON (66215-403-01) / 10 mL in 1 VIAL · 66215-403-01
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →