| NDC Code | 65219-020-23 |
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| Package Description | 10 VIAL in 1 CARTON (65219-020-23) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (65219-020-03) |
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| Product NDC | 65219-020 |
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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 | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20191031 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA062797 |
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| Manufacturer | Fresenius Kabi USA, LLC |
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| Substance Name | AMPICILLIN SODIUM |
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| Strength | 2 |
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| Strength Unit | g/1 |
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| Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS] |
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