CELECOXIB
Summary
FDA approved CELECOXIB by YILING. ANDA (Generic) approval (Labeling) on 2025-10-15. CAPSULE, ORAL.
Details
Source
Drug Approval
External ID
ANDA211412-1
Action Date
2025-10-15
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
CELECOXIB, CAPSULE, ORAL. Application: ANDA211412
Company
Context & Analysis
YILING has 5 FDA actions in our database.
Frequently Asked Questions
How often does YILING have FDA actions?
YILING 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 "ANDA211412-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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