| NDC Code | 0703-4685-01 |
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| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0703-4685-01) / 10 mL in 1 VIAL, MULTI-DOSE |
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| Product NDC | 0703-4685 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Mitoxantrone |
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| Non-Proprietary Name | Mitoxantrone |
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| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20060411 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077356 |
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| Manufacturer | Teva Parenteral Medicines, Inc. |
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| Substance Name | MITOXANTRONE HYDROCHLORIDE |
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| Strength | 2 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Topoisomerase Inhibitor [EPC], Topoisomerase Inhibitors [MoA] |
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