FdaApplication
NDA 021492
Identifiers
- fda_app_no: NDA021492
Properties
| Property | Value |
|---|---|
| applicant_name | SANOFI AVENTIS US LLC |
| application_type | NDA |
| approval_date | 2002-08-09 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ELOXATIN | OXALIPLATIN | 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INTRAVENOUS |
| ELOXATIN | OXALIPLATIN | 100MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INTRAVENOUS |
2 products