| NDC Code | 0143-9876-10 |
| Package Description | 10 BOTTLE in 1 CARTON (0143-9876-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE (0143-9876-01) |
| Product NDC | 0143-9876 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Proprietary Name | Cefoxitin |
| Non-Proprietary Name | Cefoxitin |
| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
| Usage | INTRAVENOUS |
| Start Marketing Date | 20100226 |
| Marketing Category Name | ANDA |
| Application Number | ANDA065239 |
| Manufacturer | Hikma Pharmaceuticals USA Inc. |
| Substance Name | CEFOXITIN SODIUM |
| Strength | 10 |
| Strength Unit | g/1 |
| Pharmacy Classes | Cephalosporin Antibacterial [EPC], Cephalosporins [CS] |