| NDC Code | 55390-805-10 |
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| Package Description | 10 VIAL in 1 BOX (55390-805-10) > 4 mL in 1 VIAL |
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| Product NDC | 55390-805 |
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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, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 19960628 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA064103 |
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| Manufacturer | Bedford Laboratories |
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| Substance Name | DAUNORUBICIN |
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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 [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] |
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