FDA Approved Products

Application #TypeSponsorNotesProduct #Drug NameFormStrengthActive IngredientApproval DateMarketing StatusReference Standard
213005NDALIQUIDIA TECH001YUTREPIAPOWDER;INHALATIONEQ 0.0265MG BASE/INHTREPROSTINIL SODIUM2025-05-23PrescriptionYes
002YUTREPIAPOWDER;INHALATIONEQ 0.053MG BASE/INHTREPROSTINIL SODIUM2025-05-23PrescriptionYes
003YUTREPIAPOWDER;INHALATIONEQ 0.0795MG BASE/INHTREPROSTINIL SODIUM2025-05-23PrescriptionYes
004YUTREPIAPOWDER;INHALATIONEQ 0.106MG BASE/INHTREPROSTINIL SODIUM2025-05-23PrescriptionYes