FdaApplication
ANDA 218691
Identifiers
- fda_app_no: ANDA218691
Properties
| Property | Value |
|---|---|
| applicant_name | FDC LTD |
| application_type | ANDA |
| approval_date | 2026-05-14 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CEFIXIME | CEFIXIME | 100MG/5ML | FOR SUSPENSION;ORAL |
| CEFIXIME | CEFIXIME | 200MG/5ML | FOR SUSPENSION;ORAL |
2 products