| NDC Code | 47335-046-40 |
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| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (47335-046-40) > 10 mL in 1 VIAL, SINGLE-USE |
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| Product NDC | 47335-046 |
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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 | 20140409 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202922 |
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| Manufacturer | Sun Pharmaceutical Industries, 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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