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Treprostinil

NDC 43598-646 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerDr.Reddy's Laboratories Inc.,
Marketing categoryAbbreviated NDA (generic) · App ANDA210214
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS SUBCUTANEOUS
Active ingredientsTREPROSTINIL (50 mg/20mL)
Marketing started20230213
Package count1

External sources

Source: openFDA. Public-domain (CC0).