# Treprostinil

NDC: 0703-0686
Generic name: Treprostinil
Labeler / Manufacturer: Teva Parenteral Medicines, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20190930

FDA application: ANDA206648

## Active ingredients

- TREPROSTINIL: 100 mg/20mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0703-0686"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0703-0686
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4b2ce4aa-4302-49db-9456-c8cf0e034968