FdaApplication
ANDA 203125
Identifiers
- fda_app_no: ANDA203125
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA FARMACEUTICA PORTUGAL SA |
| application_type | ANDA |
| approval_date | 2022-09-26 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METHYLPREDNISOLONE SODIUM SUCCINATE | METHYLPREDNISOLONE SODIUM SUCCINATE | EQ 40MG BASE/VIAL | INJECTABLE;INJECTION |
| METHYLPREDNISOLONE SODIUM SUCCINATE | METHYLPREDNISOLONE SODIUM SUCCINATE | EQ 125MG BASE/VIAL | INJECTABLE;INJECTION |
2 products