FdaApplication
ANDA 215673
Identifiers
- fda_app_no: ANDA215673
Properties
| Property | Value |
|---|---|
| applicant_name | AUROBINDO PHARMA LTD |
| application_type | ANDA |
| approval_date | 2023-03-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISOLONE | PREDNISOLONE | 5MG | TABLET;ORAL |
1 product