JOURNAVX (SUZETRIGINE)
Summary
FDA approved JOURNAVX (SUZETRIGINE) by VERTEX PHARMS INC. NDA (New Drug) approval (Labeling) on 2026-01-23. TABLET, ORAL.
Details
Source
Drug Approval
External ID
NDA219209-9
Action Date
2026-01-23
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
JOURNAVX (generic: SUZETRIGINE), TABLET, ORAL. Application: NDA219209
Company
Context & Analysis
VERTEX PHARMS INC has 5 FDA actions in our database.
Frequently Asked Questions
How often does VERTEX PHARMS INC have FDA actions?
VERTEX PHARMS INC has 5 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA219209-9" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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