Skip to the page

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.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

  • 33Companies
  • 83Products
  • 9Drugs by generic name

Drugs in the Bile Acid Sequestrant class

Ranked by number of companies that list the drug.

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions8tablet, film coated; tabletGeneric drugs (ANDA)August 1, 2022
Bryant Ranch Prepack6powder, for suspension; tablet, film coatedGeneric drugs (ANDA)October 20, 2021
Epic Pharma, LLC6powder, for suspensionGeneric drugs (ANDA)December 15, 2021
Amneal Pharmaceuticals of New York LLC5tablet, film coated; suspensionGeneric drugs (ANDA)January 20, 2023
Bryant Ranch Prepack5powder, for suspension; tablet, film coatedGeneric drugs (ANDA)October 20, 2021
Ascend Laboratories, LLC4powder, for suspension; tablet, film coatedGeneric drugs (ANDA)October 20, 2021
Par Health USA, LLC4powder, for suspensionGeneric drugs (ANDA)September 15, 2005
Zydus Lifesciences Limited4powder, for suspension; tablet, film coatedGeneric drugs (ANDA)May 4, 2022
Bionpharma Inc.3tablet, film coated; tabletGeneric drugs (ANDA)September 30, 2026
Macleods Pharmaceuticals Limited3powder, for suspension; tablet, film coatedGeneric drugs (ANDA)April 18, 2025
Puracap Laboratories LLC DBA Blu Pharmaceuticals3powder, for suspensionGeneric drugs (ANDA)March 14, 2023
Zydus Pharmaceuticals USA Inc.3powder, for suspension; tablet, film coatedGeneric drugs (ANDA)October 11, 2019
American Health Packaging2tablet, film coatedGeneric drugs (ANDA)May 10, 2023
Bryant Ranch Prepack2tablet, film coated; powder, for suspensionGeneric drugs (ANDA)October 20, 2021
Chartwell RX, LLC2powderGeneric drugs (ANDA)August 15, 1996
Glenmark Pharmaceuticals Inc., USA2tablet, film coated; powder, for suspensionGeneric drugs (ANDA)July 16, 2018
Mylan Pharmaceuticals Inc.2granule, for suspension; tabletAuthorized generics (NDA)July 19, 1994
Pharmacia & Upjohn Company LLC2tablet; granule, for suspensionNew drug applications (NDA)July 19, 1994
Precision Dose, Inc.2powder, for suspensionGeneric drugs (ANDA)April 25, 2024
Tagi Pharma, Inc.2powder, for suspensionGeneric drugs (ANDA)March 10, 2021
AiPing Pharmaceutical, Inc.1powder, for suspensionGeneric drugs (ANDA)September 1, 2026
Ajanta Pharma USA Inc.1powder, for suspensionGeneric drugs (ANDA)April 6, 2020
Ani Pharmaceuticals, Inc.1tablet, film coatedGeneric drugs (ANDA)May 15, 2023
Cranbury Pharmaceuticals, LLC1tabletGeneric drugs (ANDA)October 19, 2020
Dr. Reddy's Laboratories Inc.1tabletGeneric drugs (ANDA)October 5, 2018
Edenbridge Pharmaceuticals LLC.1tabletGeneric drugs (ANDA)November 26, 2024
Golden State Medical Supply, Inc.1tabletGeneric drugs (ANDA)July 15, 2020
Ingenus Pharmaceuticals, LLC1tablet, film coatedGeneric drugs (ANDA)December 3, 2024
Micro Labs Limited1powder, for suspensionGeneric drugs (ANDA)April 1, 2026
NorthStar RxLLC1tablet, film coatedGeneric drugs (ANDA)September 1, 2026
PD-Rx Pharmaceuticals, Inc.1tablet, film coatedGeneric drugs (ANDA)October 6, 2018
Upsher-Smith Laboratories, LLC1powder, for suspensionGeneric drugs (ANDA)February 1, 1996
Zydus Pharmaceuticals USA Inc.1tablet, film coatedGeneric drugs (ANDA)May 4, 2022

Dosage forms

Dosage formProductsShare
Powder, for suspension4149.4%
Tablet, film coated2530.1%
Tablet1012%
Granule, for suspension22.4%
Powder22.4%
Suspension22.4%
For suspension11.2%

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.