FdaApplication
NDA 017469
Identifiers
- fda_app_no: NDA017469
Properties
| Property | Value |
|---|---|
| applicant_name | SANDOZ INC |
| application_type | NDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OMNIPRED | PREDNISOLONE ACETATE | 1% | SUSPENSION/DROPS;OPHTHALMIC |
1 product