| NDC Code | 70594-084-02 |
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| Package Description | 10 VIAL in 1 CARTON (70594-084-02) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (70594-084-01) |
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| Product NDC | 70594-084 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ampicillin |
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| Non-Proprietary Name | Ampicillin Sodium |
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| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20210110 |
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| End Marketing Date | 20251231 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090583 |
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| Manufacturer | Xellia Pharmaceuticals USA LLC |
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| Substance Name | AMPICILLIN SODIUM |
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| Strength | 250 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS] |
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