| NDC Code | 71288-152-04 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (71288-152-04) / 4 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 71288-152 |
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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 | 20250513 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA213768 |
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| Manufacturer | Meitheal Pharmaceuticals Inc. |
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| Substance Name | DOCETAXEL |
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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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