| NDC Code | 0703-3985-01 |
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| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (0703-3985-01) / 10 mL in 1 VIAL, SINGLE-USE |
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| Product NDC | 0703-3985 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Oxaliplatin |
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| Non-Proprietary Name | Oxaliplatin |
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| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20090811 |
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| End Marketing Date | 20260331 |
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| Marketing Category Name | NDA |
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| Application Number | NDA022160 |
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| Manufacturer | Teva Parenteral Medicines, Inc. |
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| Substance Name | OXALIPLATIN |
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| Strength | 50 |
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| Strength Unit | mg/10mL |
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| Pharmacy Classes | Platinum-based Drug [EPC], Platinum-containing Compounds [EXT] |
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