| NDC Code | 42658-007-01 |
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| Package Description | 1 VIAL in 1 BOX (42658-007-01) > 4 mL in 1 VIAL |
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| Product NDC | 42658-007 |
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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, POWDER, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20161001 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | Halison Pharmaceuiticals USA, Inc |
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| Substance Name | DAUNORUBICIN HYDROCHLORIDE |
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| Strength | 20 |
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| Strength Unit | mg/4mL |
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| Pharmacy Classes | Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] |
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