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🏅 FDA Orphan Designation

Rituxan SC

rituximab and recombinant human hyaluronidase

Manufacturer: Genentech, Inc.

Indicated for:
T-cell prolymphocytic leukemiaOrphanDiffuse large B-cell lymphomaFollicular lymphoma

FDA-Approved Indications (3)

Treatment of adult patients with previously untreated and previously treated CLL in combination with fludarabine and cyclophosphamide

Treatment of adult patients with previously untreated diffuse large B-cell lymphoma in combination with cyclophosphamide, doxorubicin, vincristine, prednisone (CHOP) or other anthracycline-based chemo

Population: adults

Treatment of adult patients with relapsed or refractory, follicular lymphoma as a single agent; previously untreated follicular lymphoma in combination with first line chemotherapy and, in patients ac

Population: adults

Indications & Usage

Treatment of adult patients with previously untreated and previously treated CLL in combination with fludarabine and cyclophosphamide ||| Treatment of adult patients with previously untreated diffuse large B-cell lymphoma in combination with cyclophosphamide, doxorubicin, vincristine, prednisone (CHOP) or other anthracycline-based chemotherapy regimens ||| Treatment of adult patients with relapsed or refractory, follicular lymphoma as a single agent; previously untreated follicular lymphoma in combination with first line chemotherapy and, in patients achieving a complete or partial response to rituximab in combination with chemotherapy, as single-agent maintenance therapy; and non-progressing (including stable disease), follicular lymphoma as a single agent after first-line cyclophosphamide, vincristine, and prednisone (CVP) chemotherapy.

💙 Support Programs

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Rituxan SC
Genentech, Inc.
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Medical disclaimer: This information is for educational purposes only. Always consult a qualified healthcare provider before making treatment decisions. Data sourced from FDA and current as of our last update.