| NDC Code | 68180-822-50 |
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| Package Description | 50 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (68180-822-50) |
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| Product NDC | 68180-822 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Cefotaxime |
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| Non-Proprietary Name | Cefotaxime |
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| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20050527 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA065124 |
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| Manufacturer | Lupin Pharmaceuticals, Inc. |
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| Substance Name | CEFOTAXIME 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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