| NDC Code | 51952-012-02 |
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| Package Description | 10 VIAL in 1 VIAL (51952-012-02) > 16 mL in 1 VIAL |
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| Product NDC | 51952-012 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Zinacef |
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| Non-Proprietary Name | Cefuroxime |
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| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20130115 |
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| Marketing Category Name | APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT |
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| Application Number | NDA050558 |
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| Manufacturer | GlaxoSmithKline Manufacturing SpA |
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| Substance Name | CEFUROXIME SODIUM |
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| Strength | 90 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
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