FdaApplication
ANDA 078817
Identifiers
- fda_app_no: ANDA078817
Properties
| Property | Value |
|---|---|
| applicant_name | SANDOZ INC |
| application_type | ANDA |
| approval_date | 2011-01-24 |
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