FdaApplication
ANDA 216842
Identifiers
- fda_app_no: ANDA216842
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA PHARMS |
| application_type | ANDA |
| approval_date | 2025-01-21 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ERTUGLIFLOZIN | ERTUGLIFLOZIN | 15MG | TABLET;ORAL |
| ERTUGLIFLOZIN | ERTUGLIFLOZIN | 5MG | TABLET;ORAL |
2 products