FDA NDC Directory · JSON-LD · Markdown

Treprostinil

NDC 0703-0686 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerTeva Parenteral Medicines, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206648
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS SUBCUTANEOUS
Active ingredientsTREPROSTINIL (100 mg/20mL)
Marketing started20190930
Package count1

External sources

Source: openFDA. Public-domain (CC0).