FdaApplication
ANDA 216715
Identifiers
- fda_app_no: ANDA216715
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2022-10-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISOLONE SODIUM PHOSPHATE | PREDNISOLONE SODIUM PHOSPHATE | EQ 15MG BASE/5ML | SOLUTION;ORAL |
1 product