FdaApplication
ANDA 217174
Identifiers
- fda_app_no: ANDA217174
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2023-09-05 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CALCIUM GLUCONATE IN SODIUM CHLORIDE | CALCIUM GLUCONATE | 1GM/50ML (20MG/ML) | SOLUTION;INTRAVENOUS |
| CALCIUM GLUCONATE IN SODIUM CHLORIDE | CALCIUM GLUCONATE | 2GM/100ML (20MG/ML) | SOLUTION;INTRAVENOUS |
2 products