| NDC Code | 42658-019-01 |
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| Package Description | 1 VIAL in 1 BOX (42658-019-01) / 10 mL in 1 VIAL |
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| Product NDC | 42658-019 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Daunorubicin Hydrochloride |
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| Non-Proprietary Name | Daunorubicin Hydrochloride |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20200120 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA208759 |
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| Manufacturer | Hisun Pharmaceuticals USA, Inc. |
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| Substance Name | DAUNORUBICIN HYDROCHLORIDE |
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| Strength | 5 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Anthracycline Topoisomerase Inhibitor [EPC], Anthracyclines [CS], Topoisomerase Inhibitors [MoA] |
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