CAVHANZA
Summary
FDA approved CAVHANZA by FLEX PHARMA. NDA (New Drug) approval (Type 5 - New Formulation or New Manufacturer) on 2026-05-29. TABLET, ORALLY DISINTEGRATING, ORAL.
Details
Source
Drug Approval
External ID
NDA217379-1
Action Date
2026-05-29
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
CAVHANZA, TABLET, ORALLY DISINTEGRATING, ORAL. Application: NDA217379
Company
Context & Analysis
Frequently Asked Questions
How often does FLEX PHARMA have FDA actions?
This is the only FDA action we have on record for FLEX PHARMA in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA217379-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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