CEFIXIME
Summary
FDA approved CEFIXIME by FDC LTD. ANDA (Generic) approval on 2026-05-14. FOR SUSPENSION, ORAL.
Details
Source
Drug Approval
External ID
ANDA218691-1
Action Date
2026-05-14
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
CEFIXIME, FOR SUSPENSION, ORAL. Application: ANDA218691
Company
Context & Analysis
FDC LTD has 5 FDA actions in our database.
Frequently Asked Questions
How often does FDC LTD have FDA actions?
FDC LTD 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 "ANDA218691-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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