FDA NDC Directory · JSON-LD · Markdown

Treprostinil

NDC 0781-3430 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic nametreprostinil
Labeler / ManufacturerSandoz Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA203649
Dosage form / routeINJECTION · INTRAVENOUS SUBCUTANEOUS
Active ingredientsTREPROSTINIL (200 mg/20mL)
Marketing started20190325
Package count1

External sources

Source: openFDA. Public-domain (CC0).