| NDC Code | 47335-049-40 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 PACKAGE (47335-049-40) / 10 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 47335-049 |
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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 | 20130205 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203263 |
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| Manufacturer | Sun Pharmaceutical Industries, 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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