FdaApplication
ANDA 216493
Identifiers
- fda_app_no: ANDA216493
Properties
| Property | Value |
|---|---|
| applicant_name | HANGZHOU ZHONGMEI HUADONG PHARMACEUTICAL CO LTD |
| application_type | ANDA |
| approval_date | 2024-08-19 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FONDAPARINUX SODIUM | FONDAPARINUX SODIUM | 5MG/0.4ML (5MG/0.4ML) | SOLUTION;SUBCUTANEOUS |
| FONDAPARINUX SODIUM | FONDAPARINUX SODIUM | 10MG/0.8ML (10MG/0.8ML) | SOLUTION;SUBCUTANEOUS |
| FONDAPARINUX SODIUM | FONDAPARINUX SODIUM | 2.5MG/0.5ML (2.5MG/0.5ML) | SOLUTION;SUBCUTANEOUS |
| FONDAPARINUX SODIUM | FONDAPARINUX SODIUM | 7.5MG/0.6ML (7.5MG/0.6ML) | SOLUTION;SUBCUTANEOUS |
4 products