FdaApplication
ANDA 206697
Identifiers
- fda_app_no: ANDA206697
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2024-11-19 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| EXENATIDE SYNTHETIC | EXENATIDE SYNTHETIC | 300MCG/1.2ML (250MCG/ML) | INJECTABLE;SUBCUTANEOUS |
| EXENATIDE SYNTHETIC | EXENATIDE SYNTHETIC | 600MCG/2.4ML (250MCG/ML) | INJECTABLE;SUBCUTANEOUS |
2 products