ELIQUIS
Summary
FDA approved ELIQUIS by BRISTOL MYERS SQUIBB. NDA (New Drug) approval (Labeling) on 2026-06-24. TABLET, FOR SUSPENSION, ORAL.
Details
Source
Drug Approval
External ID
NDA202155-42
Action Date
2026-06-24
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
ELIQUIS, TABLET, FOR SUSPENSION, ORAL. Application: NDA202155
Company
Context & Analysis
BRISTOL MYERS SQUIBB has 7 FDA actions in our database.
Frequently Asked Questions
How often does BRISTOL MYERS SQUIBB have FDA actions?
BRISTOL MYERS SQUIBB has 7 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 "NDA202155-42" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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