| NDC Code | 70069-836-01 |
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| Package Description | 1 VIAL in 1 CARTON (70069-836-01) / 3.5 mL in 1 VIAL |
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| Product NDC | 70069-836 |
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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 | 20250429 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA211898 |
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| Manufacturer | Somerset Therapeutics LLC |
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| Substance Name | BORTEZOMIB |
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| Strength | 3.5 |
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| Strength Unit | mg/3.5mL |
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| Pharmacy Classes | Proteasome Inhibitor [EPC], Proteasome Inhibitors [MoA] |
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