| NDC Code | 0703-4680-01 |
|---|
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0703-4680-01) / 12.5 mL in 1 VIAL, MULTI-DOSE |
|---|
| Product NDC | 0703-4680 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Mitoxantrone |
|---|
| Non-Proprietary Name | Mitoxantrone |
|---|
| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20060411 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077356 |
|---|
| Manufacturer | Teva Parenteral Medicines, Inc. |
|---|
| Substance Name | MITOXANTRONE HYDROCHLORIDE |
|---|
| Strength | 2 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Topoisomerase Inhibitor [EPC], Topoisomerase Inhibitors [MoA] |
|---|