| NDC Code | 70121-1219-1 |
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| Package Description | 1 VIAL in 1 CARTON (70121-1219-1) / 25 mL in 1 VIAL |
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| Product NDC | 70121-1219 |
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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 | INTRAVENOUS |
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| Start Marketing Date | 20170217 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA208888 |
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| Manufacturer | Amneal Pharmaceuticals LLC |
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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 [CS], Topoisomerase Inhibitors [MoA] |
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