Data / Drug companies / Colestipol hydrochloride
Colestipol hydrochloride: 10 companies and 14 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Colestipol hydrochloride is listed in the FDA National Drug Code Directory by 10 companies, with 14 products in commercial distribution. 10 of the products (71.4%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet; granule, for suspension, and the newest product started marketing on September 1, 2026.
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- Companies listing it
- 10
- Products
- 14
- Generic (ANDA) products
- 10 (71.4%)
- Application numbers
- 8
- Routes
- Oral
- Brand names
- Colestid
- openFDA record search
- api.fda.gov
Companies that list colestipol hydrochloride
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Amneal Pharmaceuticals of New York LLC | 3 | suspension; tablet, film coated | Generic drugs (ANDA) | August 17, 2021 |
| 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 |
| American Health Packaging | 1 | tablet, film coated | Generic drugs (ANDA) | May 10, 2023 |
| Ani Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | May 15, 2023 |
| Edenbridge Pharmaceuticals LLC. | 1 | tablet | Generic drugs (ANDA) | November 26, 2024 |
| Ingenus Pharmaceuticals, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | December 3, 2024 |
| NorthStar RxLLC | 1 | tablet, film coated | Generic drugs (ANDA) | September 1, 2026 |
| Zydus Lifesciences Limited | 1 | tablet, film coated | Generic drugs (ANDA) | May 4, 2022 |
| Zydus Pharmaceuticals USA Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | May 4, 2022 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 7 | 50% |
| Tablet | 3 | 21.4% |
| Granule, for suspension | 2 | 14.3% |
| Suspension | 2 | 14.3% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 10 | 71.4% |
| New drug applications (NDA) | 2 | 14.3% |
| Authorized generics (NDA) | 2 | 14.3% |
Pharmacologic classes
| Class | Products |
|---|---|
| Bile Acid Sequestrant | 14 |
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.