FdaApplication
ANDA 218035
Identifiers
- fda_app_no: ANDA218035
Properties
| Property | Value |
|---|---|
| applicant_name | DR REDDYS LABORATORIES LTD |
| application_type | ANDA |
| approval_date | 2026-06-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISONE | PREDNISONE | 5MG | TABLET, DELAYED RELEASE;ORAL |
1 product