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Treprostinil

NDC 0781-3420 · HUMAN PRESCRIPTION DRUG · INJECTION

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

External sources

Source: openFDA. Public-domain (CC0).