ALYFTREK (VANZACAFTOR, TEZACAFTOR, AND DEUTIVACAFTOR)
Summary
FDA approved ALYFTREK (VANZACAFTOR, TEZACAFTOR, AND DEUTIVACAFTOR) by VERTEX PHARMS INC. NDA (New Drug) approval (Efficacy) on 2026-03-27. TABLET, ORAL.
Details
Source
Drug Approval
External ID
NDA218730-1
Action Date
2026-03-27
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
ALYFTREK (generic: VANZACAFTOR, TEZACAFTOR, AND DEUTIVACAFTOR), TABLET, ORAL. Application: NDA218730
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 "NDA218730-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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