| NDC Code | 68462-477-74 |
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| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (68462-477-74) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (68462-477-20) |
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| Product NDC | 68462-477 |
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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 | 20250321 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA218140 |
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| Manufacturer | GLENMARK PHARMACEUTICALS INC., USA |
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| Substance Name | VANCOMYCIN HYDROCHLORIDE |
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| Strength | 750 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Glycopeptide Antibacterial [EPC], Glycopeptides [CS] |
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