| NDC Code | 63323-821-10 |
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| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (63323-821-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE |
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| Product NDC | 63323-821 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Bortezomib |
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| Non-Proprietary Name | Bortezomib |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS; SUBCUTANEOUS |
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| Start Marketing Date | 20220502 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA209659 |
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| Manufacturer | Fresenius Kabi USA, LLC |
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| Substance Name | BORTEZOMIB |
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| Strength | 3.5 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Proteasome Inhibitor [EPC], Proteasome Inhibitors [MoA] |
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