FdaApplication
ANDA 207252
Identifiers
- fda_app_no: ANDA207252
Properties
| Property | Value |
|---|---|
| applicant_name | JIANGSU HENGRUI PHARMACEUTICALS CO LTD |
| application_type | ANDA |
| approval_date | 2017-08-09 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DOCETAXEL | DOCETAXEL | 20MG/ML (20MG/ML) | INJECTABLE;INJECTION |
| DOCETAXEL | DOCETAXEL | 80MG/4ML (20MG/ML) | INJECTABLE;INJECTION |
| DOCETAXEL | DOCETAXEL | 160MG/8ML (20MG/ML) | INJECTABLE;INJECTION |
3 products