FdaApplication
ANDA 216602
Identifiers
- fda_app_no: ANDA216602
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2024-03-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FOSCARNET SODIUM | FOSCARNET SODIUM | 6GM/250ML (24MG/ML) | SOLUTION;INTRAVENOUS |
1 product