FDA Approved Products

Application #TypeSponsorNotesProduct #Drug NameFormStrengthActive IngredientApproval DateMarketing StatusReference Standard
215515NDAALNYLAM PHARMS INC001AMVUTTRASOLUTION;SUBCUTANEOUSEQ 25MG BASE/0.5ML (EQ 25MG BASE/0.5ML)VUTRISIRAN SODIUM2022-06-13PrescriptionYes
214103NDAALNYLAM PHARMS INC001OXLUMOSOLUTION;SUBCUTANEOUSEQ 94.5MG BASE/0.5ML (EQ 94.5MG BASE/0.5ML)LUMASIRAN SODIUM2020-11-23PrescriptionYes
212194NDAALNYLAM PHARMS INC001GIVLAARISOLUTION;SUBCUTANEOUSEQ 189MG BASE/ML (EQ 189MG BASE/ML)GIVOSIRAN SODIUM2019-11-20PrescriptionYes
210922NDAALNYLAM PHARMS INC001ONPATTROSOLUTION;INTRAVENOUSEQ 10MG BASE/5ML (EQ 2MG BASE/ML)PATISIRAN SODIUM2018-08-10PrescriptionYes