FdaApplication
ANDA 217741
Identifiers
- fda_app_no: ANDA217741
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2025-03-18 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DEFLAZACORT | DEFLAZACORT | 6MG | TABLET;ORAL |
| DEFLAZACORT | DEFLAZACORT | 36MG | TABLET;ORAL |
| DEFLAZACORT | DEFLAZACORT | 30MG | TABLET;ORAL |
| DEFLAZACORT | DEFLAZACORT | 18MG | TABLET;ORAL |
4 products