| NDC Code | 70436-023-82 |
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| Package Description | 1 VIAL in 1 CARTON (70436-023-82) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
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| Product NDC | 70436-023 |
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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 | 20210206 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA215821 |
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| Manufacturer | Slate Run Pharmaceuticals, LLC |
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| Substance Name | VANCOMYCIN HYDROCHLORIDE |
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| Strength | 10 |
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| Strength Unit | g/1 |
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| Pharmacy Classes | Glycopeptide Antibacterial [EPC], Glycopeptides [CS] |
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