| NDC Code | 70594-037-01 |
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| Package Description | 1 VIAL, GLASS in 1 CARTON (70594-037-01) / 5 mL in 1 VIAL, GLASS |
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| Product NDC | 70594-037 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Micafungin |
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| Non-Proprietary Name | Micafungin Sodium |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20210602 |
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| End Marketing Date | 20251231 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA211713 |
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| Manufacturer | Xellia Pharmaceuticals USA LLC |
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| Substance Name | MICAFUNGIN SODIUM |
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| Strength | 20 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Echinocandin Antifungal [EPC], Lipopeptides [CS] |
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