| NDC Code | 0955-1021-04 |
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| Package Description | 1 VIAL, GLASS in 1 CARTON (0955-1021-04) / 4 mL in 1 VIAL, GLASS |
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| Product NDC | 0955-1021 |
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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 | 20101021 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA020449 |
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| Manufacturer | Winthrop U.S, a business of sanofi-aventis U.S. LLC |
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| Substance Name | DOCETAXEL |
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| Strength | 80 |
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| Strength Unit | mg/4mL |
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| Pharmacy Classes | Microtubule Inhibition [PE], Microtubule Inhibitor [EPC] |
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