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Each mL of concentrate contains 10 mg of rituximab.

Each vial of 50 mL contains 500 mg of rituximab.
Each vial of 10 mL contains 100 mg of rituximab.


- Truxima 500 mg concentrate for solution for infusion: Pack of 1 vial 
- Truxima 100 mg concentrate for solution for infusion: Pack of 2 vials



The registered formulation of Rituximab is 10mg/ml concentrate for solution for intravenous (IV) infusion, and it is indicated for:

• Non-Hodgkin’s Lymphoma (NHL): Rituximab is indicated for the treatment of previously untreated patients with stage III-IV follicular lymphoma (FL) along with chemotherapy or in patients who are chemo-resistant or are in their second and subsequent relapse after  chemotherapy. It is also given in patients with CD20 positive large B cell NHL in combination with cyclophosphamide, doxorubicin, vincristine, prednisolone chemotherapy. Additionally, maintenance therapy is indicated for the treatment of FL individuals responding to induction therapy.
• Chronic Lymphocytic Leukaemia (CLL): Rituximab is indicated for the  treatment of patients with previously untreated and relapsed CLL in combination with chemotherapy.
• Rheumatoid Arthritis (RA): Rituximab in combination with methotrexate is given to the adult patient with severe active RA who had insufficient response or intolerance to other disease-modifying anti-rheumatic drugs (DMARD) including one or more tumour necrosis factor inhibitor (TNFi) therapies.
• Granulomatosis with Polyangiitis and Microscopic Polyangiitis (GPA/MPA): In combination with glucocorticoids, Rituximab is given for the induction of remission in adult patients with severe, active GPA/MPA.