| NDC Code | 55390-108-01 |
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| Package Description | 1 VIAL in 1 BOX, UNIT-DOSE (55390-108-01) > 10 mL in 1 VIAL |
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| Product NDC | 55390-108 |
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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 |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 19980601 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA050731 |
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| Manufacturer | Bedford Laboratories |
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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 [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] |
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