| NDC Code | 52584-332-01 |
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| Package Description | 1 VIAL in 1 BAG (52584-332-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
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| Product NDC | 52584-332 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Vancomycin Hydrochloride |
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| Non-Proprietary Name | Vancomycin Hydrochloride |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20100901 |
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| End Marketing Date | 20240101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA062911 |
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| Manufacturer | General Injectables & Vaccines, Inc |
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| Substance Name | VANCOMYCIN HYDROCHLORIDE |
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| Strength | 500 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Glycopeptide Antibacterial [EPC], Glycopeptides [CS] |
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