| NDC Code | 0703-5720-01 |
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| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (0703-5720-01) > 1 mL in 1 VIAL, SINGLE-USE |
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| Product NDC | 0703-5720 |
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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 | 20151231 |
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| End Marketing Date | 20181130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203877 |
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| Manufacturer | Teva Parenteral Medicines, Inc. |
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| Substance Name | DOCETAXEL ANHYDROUS |
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| Strength | 20 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Microtubule Inhibition [PE],Microtubule Inhibitor [EPC] |
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