FdaApplication
ANDA 078818
Identifiers
- fda_app_no: ANDA078818
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2009-08-07 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXALIPLATIN | OXALIPLATIN | 100MG/VIAL | INJECTABLE;INTRAVENOUS |
| OXALIPLATIN | OXALIPLATIN | 50MG/VIAL | INJECTABLE;INTRAVENOUS |
2 products