FdaApplication
ANDA 203869
Identifiers
- fda_app_no: ANDA203869
Properties
| Property | Value |
|---|---|
| applicant_name | JIANGSU HENGRUI PHARMACEUTICALS CO LTD |
| application_type | ANDA |
| approval_date | 2014-06-18 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXALIPLATIN | OXALIPLATIN | 100MG/20ML (5MG/ML) | INJECTABLE;INTRAVENOUS |
| OXALIPLATIN | OXALIPLATIN | 50MG/10ML (5MG/ML) | INJECTABLE;INTRAVENOUS |
2 products