TRYNGOLZA (AUTOINJECTOR)
OLEZARSEN SODIUM
Approval overview TRYNGOLZA (AUTOINJECTOR) is listed in Drugs@FDA under application 218614 (NDA).
Review priority: PRIORITY Marketing status: Prescription Active ingredient OLEZARSEN SODIUM Form and strength SOLUTION;SUBCUTANEOUS - EQ 80MG BASE/0.8ML (EQ 80MG BASE/0.8ML) Sponsor IONIS PHARMS INC Submission history Latest submission status date: 2024-12-19 00:00:00.
Structured Monograph
Clinical summary
Approval overview TRYNGOLZA (AUTOINJECTOR) is listed in Drugs@FDA under application 218614 (NDA). Review priority: PRIORITY Marketing status: Prescription Active ingredient OLEZARSEN SODIUM Form and strength SOLUTION;SUBCUTANEOUS - EQ 80MG BASE/0.8ML (EQ 80MG BASE/0.8ML) Sponsor IONIS PHARMS INC Submission history Latest submission status date: 2024-12-19 00:00:00. Submission type: ORIG.
Monitoring
- • Marketing status: Prescription
- • Review priority: PRIORITY
Interaction Notes
- No interaction notes stored yet.