# Treprostinil

NDC: 0781-3430
Generic name: treprostinil
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20190325

FDA application: ANDA203649

## Active ingredients

- TREPROSTINIL: 200 mg/20mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-3430"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-3430
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=473297ca-a872-4052-a053-87dc8f0d3c13