| NDC Code | 51991-218-98 |
|---|
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (51991-218-98) > 10 mL in 1 VIAL, SINGLE-DOSE |
|---|
| Product NDC | 51991-218 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Oxaliplatin |
|---|
| Non-Proprietary Name | Oxaliplatin |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20170901 |
|---|
| End Marketing Date | 20201031 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA204616 |
|---|
| Manufacturer | Breckenridge Pharmaceutical, Inc. |
|---|
| Substance Name | OXALIPLATIN |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/10mL |
|---|
| Pharmacy Classes | Platinum-based Drug [EPC],Platinum-containing Compounds [EXT] |
|---|