FdaApplication
ANDA 074511
Identifiers
- fda_app_no: ANDA074511
Properties
| Property | Value |
|---|---|
| applicant_name | EPIC PHARMA LLC |
| application_type | ANDA |
| approval_date | 1996-07-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SULSTER | PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM | EQ 0.23% PHOSPHATE;10% | SOLUTION/DROPS;OPHTHALMIC |
1 product