FdaApplication
ANDA 212700
Identifiers
- fda_app_no: ANDA212700
Properties
| Property | Value |
|---|---|
| applicant_name | JIANGSU HENGRUI PHARMACEUTICALS CO LTD |
| application_type | ANDA |
| approval_date | 2024-10-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PACLITAXEL | PACLITAXEL | 100MG/VIAL | POWDER;INTRAVENOUS |
1 product