| NDC Code | 16714-742-01 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (16714-742-01) / 10 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 16714-742 |
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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 | INJECTABLE, LIPOSOMAL |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20170829 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA208657 |
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| Manufacturer | NorthStar RxLLC |
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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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