FdaApplication
ANDA 211451
Identifiers
- fda_app_no: ANDA211451
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA PHARMACEUTICALS INTERNATIONAL LTD |
| application_type | ANDA |
| approval_date | 2023-08-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DEXAMETHASONE SODIUM PHOSPHATE | DEXAMETHASONE SODIUM PHOSPHATE | EQ 4MG PHOSPHATE/ML | INJECTABLE;INJECTION |
1 product