FdaApplication
ANDA 081043
Identifiers
- fda_app_no: ANDA081043
Properties
| Property | Value |
|---|---|
| applicant_name | ALCON PHARMACEUTICALS LTD |
| application_type | ANDA |
| approval_date | 1991-10-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISOLONE SODIUM PHOSPHATE | PREDNISOLONE SODIUM PHOSPHATE | EQ 0.11% PHOSPHATE | SOLUTION/DROPS;OPHTHALMIC |
1 product