Data / Drug companies / CD20-directed Cytolytic Antibody
CD20-directed Cytolytic Antibody drugs: 10 drugs from 6 companies in the FDA NDC directory
CD20-directed Cytolytic Antibody is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 15 products in this class from 6 companies, covering 10 drugs by generic name. The main marketing category is biologics (BLA), and the newest product started marketing on September 13, 2024.
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- 6Companies
- 15Products
- 10Drugs by generic name
Drugs in the CD20-directed Cytolytic Antibody class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Rituximab | 2 | 1 |
| Rituximab and hyaluronidase | 2 | 1 |
| Rituximab-abbs | 2 | 1 |
| Rituximab-arrx | 2 | 1 |
| Rituximab-pvvr | 2 | 1 |
| Obinutuzumab | 1 | 1 |
| Ocrelizumab | 1 | 1 |
| Ocrelizumab and hyaluronidase | 1 | 1 |
| Ofatumumab | 1 | 1 |
| Ublituximab | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Genentech, Inc. | 7 | injection, solution; injection, solution, concentrate | Biologics (BLA) | September 13, 2024 |
| Amgen, Inc | 2 | injection, solution | Biologics (BLA) | January 6, 2021 |
| Cephalon, LLC | 2 | injection, solution | Biologics (BLA) | May 4, 2020 |
| Pfizer Laboratories Div Pfizer Inc | 2 | injection, solution | Biologics (BLA) | January 23, 2020 |
| Novartis Pharmaceuticals Corporation | 1 | injection, solution | Biologics (BLA) | October 26, 2009 |
| TG Therapeutics, Inc. | 1 | injection, solution, concentrate | Biologics (BLA) | December 28, 2022 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection, solution | 12 | 80% |
| Injection, solution, concentrate | 2 | 13.3% |
| Injection | 1 | 6.7% |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.