FdaApplication
ANDA 083362
Identifiers
- fda_app_no: ANDA083362
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1984-02-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISOLONE TEBUTATE | PREDNISOLONE TEBUTATE | 20MG/ML | INJECTABLE;INJECTION |
1 product