FdaApplication
ANDA 085781
Identifiers
- fda_app_no: ANDA085781
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISOLONE ACETATE | PREDNISOLONE ACETATE | 50MG/ML | INJECTABLE;INJECTION |
1 product