| NDC Code | 0069-0080-01 |
|---|
| Package Description | 10 mL in 1 VIAL (0069-0080-01) |
|---|
| Product NDC | 0069-0080 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Mitoxantrone Hydrochloride |
|---|
| Non-Proprietary Name | Mitoxantrone Hydrochloride |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20121212 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA201014 |
|---|
| Manufacturer | Pfizer Laboratories Div Pfizer Inc. |
|---|
| Substance Name | MITOXANTRONE HYDROCHLORIDE |
|---|
| Strength | 2 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Topoisomerase Inhibitor [EPC],Topoisomerase Inhibitors [MoA] |
|---|