FDA NDC

Veletri

This name is from the loaded FDA file.

Source: FDA NDC Directory, live from openFDA. Publisher page

NDC
66215-402
Proprietary name
Veletri
Nonproprietary name
epoprostenol
Labeler
Actelion Pharmaceuticals US, Inc.
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Strength
1.5 mg/10mL

Run it in Rivvi

Which 2027 plans near you dropped or restricted epoprostenol?

Tier changes and new prior auth, step therapy or quantity limits, plan by plan, from the CMS Part D files.

Free to start. Opens Rivvi, the AI workspace for healthcare teams.

Try it on your own data today.

Free to start. Most teams are using it the same day.