| NDC Code | 0409-0812-01 |
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| Package Description | 25 VIAL, PATENT DELIVERY SYSTEM in 1 CARTON (0409-0812-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PATENT DELIVERY SYSTEM |
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| Product NDC | 0409-0812 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Cefotaxime |
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| Non-Proprietary Name | Cefotaxime |
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| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20160219 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203132 |
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| Manufacturer | Hospira, Inc. |
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| Substance Name | CEFOTAXIME SODIUM |
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| Strength | 2 |
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| Strength Unit | g/1 |
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| Pharmacy Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
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