YUVEZZI (CARBACHOL AND BRIMONIDINE TARTRATE)
Summary
FDA approved YUVEZZI (CARBACHOL AND BRIMONIDINE TARTRATE) by VISUS. NDA (New Drug) approval (Type 3 - New Dosage Form and Type 4 - New Combination) on 2026-01-28. SOLUTION/DROPS, OPHTHALMIC.
Details
Source
Drug Approval
External ID
NDA220142-1
Action Date
2026-01-28
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
YUVEZZI (generic: CARBACHOL AND BRIMONIDINE TARTRATE), SOLUTION/DROPS, OPHTHALMIC. Application: NDA220142
Company
Context & Analysis
Frequently Asked Questions
How often does VISUS have FDA actions?
This is the only FDA action we have on record for VISUS in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA220142-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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