FdaApplication
ANDA 088678
Identifiers
- fda_app_no: ANDA088678
Properties
| Property | Value |
|---|---|
| applicant_name | ABRAXIS PHARMACEUTICAL PRODUCTS |
| application_type | ANDA |
| approval_date | 1984-06-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METHYLPREDNISOLONE SODIUM SUCCINATE | METHYLPREDNISOLONE SODIUM SUCCINATE | EQ 500MG BASE/VIAL | INJECTABLE;INJECTION |
1 product