FdaApplication
ANDA 083358
Identifiers
- fda_app_no: ANDA083358
Properties
| Property | Value |
|---|---|
| applicant_name | EPIC PHARMA LLC |
| application_type | ANDA |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISOLONE SODIUM PHOSPHATE | PREDNISOLONE SODIUM PHOSPHATE | EQ 0.9% PHOSPHATE | SOLUTION/DROPS;OPHTHALMIC |
| PREDNISOLONE SODIUM PHOSPHATE | PREDNISOLONE SODIUM PHOSPHATE | EQ 0.11% PHOSPHATE | SOLUTION/DROPS;OPHTHALMIC |
2 products