| NDC Code | 0409-0124-01 |
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| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (0409-0124-01) > 25 mL in 1 VIAL, SINGLE-USE |
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| Product NDC | 0409-0124 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Doxorubicin Hydrochloride |
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| Non-Proprietary Name | Doxorubicin Hydrochloride |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRA-ARTERIAL; INTRAVENOUS; INTRAVESICAL |
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| Start Marketing Date | 20160418 |
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| End Marketing Date | 20171231 |
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| Marketing Category Name | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
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| Manufacturer | Hospira, Inc. |
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| Substance Name | DOXORUBICIN HYDROCHLORIDE |
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| Strength | 2 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] |
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