| NDC Code | 63323-352-45 |
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| Package Description | 25 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (63323-352-45) |
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| Product NDC | 63323-352 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Cefuroxime |
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| Non-Proprietary Name | Cefuroxime |
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| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20110524 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA064125 |
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| Manufacturer | APP Pharmaceuticals, LLC |
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| Substance Name | CEFUROXIME |
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| Strength | 750 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
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