Data / Drug companies / Bile Acid Sequestrant
Bile Acid Sequestrant drugs: 9 drugs from 33 companies in the FDA NDC directory
Bile Acid Sequestrant is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 83 products in this class from 33 companies, covering 9 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on September 30, 2026.
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- 33Companies
- 83Products
- 9Drugs by generic name
Drugs in the Bile Acid Sequestrant class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Cholestyramine | 26 | 14 |
| Colesevelam hydrochloride | 21 | 12 |
| Colestipol hydrochloride | 14 | 10 |
| Colesevelam hcl | 7 | 6 |
| Cholestyramine powder for suspension | 4 | 4 |
| Cholestyramine light | 5 | 2 |
| Choleystyramine light | 2 | 2 |
| Colesevelam | 2 | 2 |
| Cholestyramine for oral suspension | 2 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| A-S Medication Solutions | 8 | tablet, film coated; tablet | Generic drugs (ANDA) | August 1, 2022 |
| Bryant Ranch Prepack | 6 | powder, for suspension; tablet, film coated | Generic drugs (ANDA) | October 20, 2021 |
| Epic Pharma, LLC | 6 | powder, for suspension | Generic drugs (ANDA) | December 15, 2021 |
| Amneal Pharmaceuticals of New York LLC | 5 | tablet, film coated; suspension | Generic drugs (ANDA) | January 20, 2023 |
| Bryant Ranch Prepack | 5 | powder, for suspension; tablet, film coated | Generic drugs (ANDA) | October 20, 2021 |
| Ascend Laboratories, LLC | 4 | powder, for suspension; tablet, film coated | Generic drugs (ANDA) | October 20, 2021 |
| Par Health USA, LLC | 4 | powder, for suspension | Generic drugs (ANDA) | September 15, 2005 |
| Zydus Lifesciences Limited | 4 | powder, for suspension; tablet, film coated | Generic drugs (ANDA) | May 4, 2022 |
| Bionpharma Inc. | 3 | tablet, film coated; tablet | Generic drugs (ANDA) | September 30, 2026 |
| Macleods Pharmaceuticals Limited | 3 | powder, for suspension; tablet, film coated | Generic drugs (ANDA) | April 18, 2025 |
| Puracap Laboratories LLC DBA Blu Pharmaceuticals | 3 | powder, for suspension | Generic drugs (ANDA) | March 14, 2023 |
| Zydus Pharmaceuticals USA Inc. | 3 | powder, for suspension; tablet, film coated | Generic drugs (ANDA) | October 11, 2019 |
| American Health Packaging | 2 | tablet, film coated | Generic drugs (ANDA) | May 10, 2023 |
| Bryant Ranch Prepack | 2 | tablet, film coated; powder, for suspension | Generic drugs (ANDA) | October 20, 2021 |
| Chartwell RX, LLC | 2 | powder | Generic drugs (ANDA) | August 15, 1996 |
| Glenmark Pharmaceuticals Inc., USA | 2 | tablet, film coated; powder, for suspension | Generic drugs (ANDA) | July 16, 2018 |
| Mylan Pharmaceuticals Inc. | 2 | granule, for suspension; tablet | Authorized generics (NDA) | July 19, 1994 |
| Pharmacia & Upjohn Company LLC | 2 | tablet; granule, for suspension | New drug applications (NDA) | July 19, 1994 |
| Precision Dose, Inc. | 2 | powder, for suspension | Generic drugs (ANDA) | April 25, 2024 |
| Tagi Pharma, Inc. | 2 | powder, for suspension | Generic drugs (ANDA) | March 10, 2021 |
| AiPing Pharmaceutical, Inc. | 1 | powder, for suspension | Generic drugs (ANDA) | September 1, 2026 |
| Ajanta Pharma USA Inc. | 1 | powder, for suspension | Generic drugs (ANDA) | April 6, 2020 |
| Ani Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | May 15, 2023 |
| Cranbury Pharmaceuticals, LLC | 1 | tablet | Generic drugs (ANDA) | October 19, 2020 |
| Dr. Reddy's Laboratories Inc. | 1 | tablet | Generic drugs (ANDA) | October 5, 2018 |
| Edenbridge Pharmaceuticals LLC. | 1 | tablet | Generic drugs (ANDA) | November 26, 2024 |
| Golden State Medical Supply, Inc. | 1 | tablet | Generic drugs (ANDA) | July 15, 2020 |
| Ingenus Pharmaceuticals, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | December 3, 2024 |
| Micro Labs Limited | 1 | powder, for suspension | Generic drugs (ANDA) | April 1, 2026 |
| NorthStar RxLLC | 1 | tablet, film coated | Generic drugs (ANDA) | September 1, 2026 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | October 6, 2018 |
| Upsher-Smith Laboratories, LLC | 1 | powder, for suspension | Generic drugs (ANDA) | February 1, 1996 |
| Zydus Pharmaceuticals USA Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | May 4, 2022 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Powder, for suspension | 41 | 49.4% |
| Tablet, film coated | 25 | 30.1% |
| Tablet | 10 | 12% |
| Granule, for suspension | 2 | 2.4% |
| Powder | 2 | 2.4% |
| Suspension | 2 | 2.4% |
| For suspension | 1 | 1.2% |
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.