| NDC Code | 63323-729-12 |
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| Package Description | 10 CARTON in 1 CARTON (63323-729-12) / 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-729-02) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 63323-729 |
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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 | 20200508 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA207344 |
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| Manufacturer | Fresenius Kabi USA, LLC |
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| Substance Name | MICAFUNGIN SODIUM |
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| Strength | 100 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Echinocandin Antifungal [EPC], Lipopeptides [CS] |
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