# Orenitram

NDC: 66302-361
Generic name: treprostinil
Labeler / Manufacturer: United Therapeutics Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: KIT
Routes: —
Marketing started: 20230214

FDA application: NDA203496

## Active ingredients

—

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"66302-361"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=66302-361
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8ed2003a-c801-411e-831e-d06079bb0d7c