| NDC Code | 79672-825-02 |
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| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (79672-825-02) / 10 mL in 1 VIAL, SINGLE-USE |
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| Product NDC | 79672-825 |
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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, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20200701 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204616 |
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| Manufacturer | Nextgen Pharmaceuticals LLC |
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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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