| NDC Code | 50242-108-86 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (50242-108-86) / 11.7 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 50242-108 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Rituxan Hycela |
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| Non-Proprietary Name | Rituximab And Hyaluronidase |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | SUBCUTANEOUS |
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| Start Marketing Date | 20170622 |
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| Marketing Category Name | BLA |
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| Application Number | BLA761064 |
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| Manufacturer | Genentech, Inc. |
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| Substance Name | HYALURONIDASE (HUMAN RECOMBINANT); RITUXIMAB |
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| Strength | 2000; 120 |
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| Strength Unit | U/mL; mg/mL |
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| Pharmacy Classes | CD20-directed Antibody Interactions [MoA], CD20-directed Cytolytic Antibody [EPC], Endoglycosidase [EPC], Glycoside Hydrolases [CS] |
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