FdaApplication
ANDA 203559
Identifiers
- fda_app_no: ANDA203559
Properties
| Property | Value |
|---|---|
| applicant_name | EDENBRIDGE PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2016-12-20 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISOLONE SODIUM PHOSPHATE | PREDNISOLONE SODIUM PHOSPHATE | EQ 20MG BASE/5ML | SOLUTION;ORAL |
| PREDNISOLONE SODIUM PHOSPHATE | PREDNISOLONE SODIUM PHOSPHATE | EQ 25MG BASE/5ML | SOLUTION;ORAL |
| PREDNISOLONE SODIUM PHOSPHATE | PREDNISOLONE SODIUM PHOSPHATE | EQ 15MG BASE/5ML | SOLUTION;ORAL |
| PREDNISOLONE SODIUM PHOSPHATE | PREDNISOLONE SODIUM PHOSPHATE | EQ 10MG BASE/5ML | SOLUTION;ORAL |
4 products