| NDC Code | 0069-9141-22 |
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| Package Description | 1 VIAL, PLASTIC in 1 CARTON (0069-9141-22) > 2 mL in 1 VIAL, PLASTIC |
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| Product NDC | 0069-9141 |
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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 | 20140623 |
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| Marketing Category Name | NDA |
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| Application Number | NDA202356 |
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| Manufacturer | Pfizer Laboratories Div Pfizer Inc |
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| Substance Name | DOCETAXEL ANHYDROUS |
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| Strength | 20 |
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| Strength Unit | mg/2mL |
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| Pharmacy Classes | Microtubule Inhibition [PE],Microtubule Inhibitor [EPC] |
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