| NDC Code | 25021-135-10 |
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| Package Description | 10 VIAL in 1 CARTON (25021-135-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
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| Product NDC | 25021-135 |
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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 |
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| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20140701 |
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| End Marketing Date | 20220331 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090354 |
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| Manufacturer | Sagent Pharmaceuticals |
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| Substance Name | AMPICILLIN SODIUM |
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| Strength | 500 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS] |
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