| NDC Code | 0143-9878-25 |
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| Package Description | 25 VIAL in 1 CARTON (0143-9878-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9878-01) |
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| Product NDC | 0143-9878 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Cefoxitin |
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| Non-Proprietary Name | Cefoxitin |
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| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20100312 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA065238 |
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| Manufacturer | Hikma Pharmaceuticals USA Inc. |
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| Substance Name | CEFOXITIN SODIUM |
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| Strength | 1 |
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| Strength Unit | g/1 |
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| Pharmacy Classes | Cephalosporin Antibacterial [EPC], Cephalosporins [CS] |
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