| NDC Code | 57884-3021-0 |
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| Package Description | 1 BLISTER PACK in 1 CARTON (57884-3021-0) > 2 VIAL, GLASS in 1 BLISTER PACK > .5 mL in 1 VIAL, GLASS |
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| Product NDC | 57884-3021 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Docetaxel |
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| Non-Proprietary Name | Docetaxel |
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| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20170215 |
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| End Marketing Date | 20211029 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203170 |
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| Manufacturer | Jiangsu Hengrui Pharmaceuticals Co., Ltd. |
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| Substance Name | DOCETAXEL |
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| Strength | 40 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Microtubule Inhibition [PE],Microtubule Inhibitor [EPC] |
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