FdaApplication
ANDA 206358
Identifiers
- fda_app_no: ANDA206358
Properties
| Property | Value |
|---|---|
| applicant_name | FDC LTD |
| application_type | ANDA |
| approval_date | 2024-12-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CEFIXIME | CEFIXIME | 400MG | TABLET;ORAL |
1 product