FdaApplication
ANDA 216920
Identifiers
- fda_app_no: ANDA216920
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2024-03-15 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM ACETATE | SODIUM ACETATE | 200MEQ/100ML (2MEQ/ML) | SOLUTION;INTRAVENOUS |
| SODIUM ACETATE | SODIUM ACETATE | 40MEQ/20ML (2MEQ/ML) | SOLUTION;INTRAVENOUS |
| SODIUM ACETATE | SODIUM ACETATE | 100MEQ/50ML (2MEQ/ML) | SOLUTION;INTRAVENOUS |
3 products