FdaApplication
ANDA 213768
Identifiers
- fda_app_no: ANDA213768
Properties
| Property | Value |
|---|---|
| applicant_name | GUANGDONG SUNHO PHARMACEUTICAL CO LTD |
| application_type | ANDA |
| approval_date | 2025-05-13 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DOCETAXEL | DOCETAXEL | 20MG/ML (20MG/ML) | INJECTABLE;INJECTION |
| DOCETAXEL | DOCETAXEL | 80MG/4ML (20MG/ML) | INJECTABLE;INJECTION |
2 products