| NDC Code | 0703-5040-01 |
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| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0703-5040-01) > 100 mL in 1 VIAL, MULTI-DOSE |
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| Product NDC | 0703-5040 |
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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, SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 19960901 |
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| End Marketing Date | 20200131 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA064140 |
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| Manufacturer | Teva Parenteral Medicines, 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 [CS],Topoisomerase Inhibitors [MoA] |
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