| NDC Code | 0024-5858-22 |
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| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0024-5858-22) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (0024-5858-20) |
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| Product NDC | 0024-5858 |
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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 | 20140623 |
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| Marketing Category Name | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
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| Manufacturer | Sanofi-Aventis U.S. LLC |
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| Substance Name | DAUNORUBICIN HYDROCHLORIDE |
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| Strength | 20 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] |
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