| NDC Code | 0409-3718-01 |
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| Package Description | 10 VIAL, GLASS in 1 PACKAGE (0409-3718-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0409-3718-10) |
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| Product NDC | 0409-3718 |
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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 | 20170801 |
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| End Marketing Date | 20241130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA061395 |
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| Manufacturer | Hospira, Inc |
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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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