| NDC Code | 52584-135-10 |
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| Package Description | 1 VIAL in 1 BAG (52584-135-10) > 500 mg in 1 VIAL |
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| Product NDC | 52584-135 |
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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 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 | 20130313 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA063146 |
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| Manufacturer | General Injectables & Vaccines, Inc |
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| Substance Name | AMPICILLIN SODIUM |
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| Strength | 500 |
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| Strength Unit | mg/500mg |
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| Pharmacy Classes | Penicillin-class Antibacterial [EPC],Penicillins [CS] |
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