| NDC Code | 68001-572-41 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (68001-572-41) / 20 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 68001-572 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Bendamustine Hydrochloride |
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| Non-Proprietary Name | Bendamustine 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 | 20230915 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA205574 |
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| Manufacturer | BluePoint Laboratories |
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| Substance Name | BENDAMUSTINE HYDROCHLORIDE |
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| Strength | 100 |
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| Strength Unit | mg/20mL |
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| Pharmacy Classes | Alkylating Activity [MoA], Alkylating Drug [EPC] |
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