| NDC Code | 68462-957-05 |
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| Package Description | 1 BOTTLE in 1 CARTON (68462-957-05) / 100 mL in 1 BOTTLE |
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| Product NDC | 68462-957 |
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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 | 20261012 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA205694 |
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| Manufacturer | GLENMARK PHARMACEUTICALS INC., USA |
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| Substance Name | VANCOMYCIN HYDROCHLORIDE |
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| Strength | 5 |
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| Strength Unit | g/100mL |
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| Pharmacy Classes | Glycopeptide Antibacterial [EPC], Glycopeptides [CS] |
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