Data / Drug companies / Tubulin Inhibiting Agent
Tubulin Inhibiting Agent drugs: 5 drugs from 9 companies in the FDA NDC directory
Tubulin Inhibiting Agent is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 21 products in this class from 9 companies, covering 5 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on June 30, 2023.
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- 9Companies
- 21Products
- 5Drugs by generic name
Drugs in the Tubulin Inhibiting Agent class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Griseofulvin | 11 | 6 |
| Ultramicrosize griseofulvin | 6 | 4 |
| Ultramicrosize griseofulvin tablets | 2 | 1 |
| Griseofulvin (microsize) | 1 | 1 |
| Grisofulvin | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Chartwell RX, LLC | 5 | tablet; suspension | Generic drugs (ANDA) | March 2, 2005 |
| Sandoz Inc | 4 | tablet, coated; tablet | Generic drugs (ANDA) | April 1, 2020 |
| Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc. | 3 | tablet | Generic drugs (ANDA) | June 30, 2023 |
| Sigmapharm Laboratories, LLC | 3 | tablet | Generic drugs (ANDA) | December 6, 2012 |
| Amneal Pharmaceuticals of New York LLC | 2 | tablet, coated | Generic drugs (ANDA) | September 29, 2014 |
| Actavis Pharma, Inc. | 1 | suspension | Generic drugs (ANDA) | July 26, 2007 |
| Ayurax, LLC | 1 | tablet | Generic drugs (ANDA) | April 6, 1982 |
| Cipla USA Inc. | 1 | suspension | Generic drugs (ANDA) | March 6, 2017 |
| Cosette Pharmaceuticals, Inc. | 1 | suspension | Generic drugs (ANDA) | November 1, 2022 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 13 | 61.9% |
| Suspension | 4 | 19% |
| Tablet, coated | 4 | 19% |
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.