50242-108 : Rituxan Hycela Subcutaneous Injection, Solution
| NDC: | 50242-108 |
| Labeler: | Genentech, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Rituxan Hycela |
| Dosage Form: | Subcutaneous Injection, Solution |
| Application #: | BLA761064 |
| Rev. Date: |
NDC Package Codes:
- 50242-108-01: 1 VIAL, SINGLE‑DOSE IN 1 CARTON (50242‑108‑01) > 11.7 ML IN 1 VIAL, SINGLE‑DOSE
- 50242-108-86: 1 VIAL, SINGLE‑DOSE IN 1 CARTON (50242‑108‑86) > 11.7 ML IN 1 VIAL, SINGLE‑DOSE
Active Ingredients:
- Rituximab
- Hyaluronidase (Human Recombinant)
Dosage Strength:
- 120 mg/mL
- 2000 U/mL
Pharmaceutical Classes:
- CD20-directed Antibody Interactions [MoA]
- CD20-directed Cytolytic Antibody [EPC]
- Endoglycosidase [EPC]
- Glycoside Hydrolases [CS]
Related Products:
Based on records with the same trade name.- 50242-109 Rituxan Hycela Subcutaneous Injection, Solution by Genentech, Inc.
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.