| NDC Code | 25021-121-66 |
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| Package Description | 10 VIAL in 1 CARTON (25021-121-66) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
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| Product NDC | 25021-121 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Cefepime |
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| Non-Proprietary Name | Cefepime Hydrochloride |
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| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20150701 |
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| End Marketing Date | 20240630 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA065441 |
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| Manufacturer | Sagent Pharmaceuticals |
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| Substance Name | CEFEPIME HYDROCHLORIDE |
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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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