| NDC Code | 47335-082-50 |
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| Package Description | 1 VIAL, SINGLE-USE in 1 PACKAGE (47335-082-50) > 10 mL in 1 VIAL, SINGLE-USE |
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| Product NDC | 47335-082 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Lipodox |
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| Non-Proprietary Name | Doxorubicin Hydrochloride |
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| Dosage Form | INJECTABLE, LIPOSOMAL |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20120209 |
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| Marketing Category Name | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
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| Manufacturer | Sun Pharma Global FZE |
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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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