Data / Drug companies / Gastrointestinal Motility Inhibitor
Gastrointestinal Motility Inhibitor drugs: 3 drugs from 7 companies in the FDA NDC directory
Gastrointestinal Motility Inhibitor is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 12 products in this class from 7 companies, covering 3 drugs by generic name. The main marketing category is new drug applications (NDA), and the newest product started marketing on August 19, 2025.
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- 7Companies
- 12Products
- 3Drugs by generic name
Drugs in the Gastrointestinal Motility Inhibitor class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Glucagon | 6 | 9 |
| Glucagon injection, solution | 4 | 1 |
| Glucagon injection | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Xeris Pharmaceuticals, Inc. | 4 | injection, solution | New drug applications (NDA) | October 11, 2021 |
| Amphastar Pharmaceuticals, Inc. | 2 | powder | New drug applications (NDA) | July 24, 2019 |
| Fresenius Kabi USA, LLC | 2 | injection, powder, lyophilized, for solution | New drug applications (NDA) | May 8, 2015 |
| American Regent, Inc. | 1 | injection, solution | New drug applications (NDA) | August 19, 2025 |
| Healthsource of New England LLC | 1 | liquid | Unapproved homeopathic products | April 11, 2018 |
| Professional Complementary Health Formulas | 1 | liquid | Unapproved homeopathic products | August 15, 1984 |
| Sportpharm LLC | 1 | powder | New drug applications (NDA) | July 24, 2019 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection, solution | 5 | 41.7% |
| Powder | 3 | 25% |
| Liquid | 2 | 16.7% |
| Injection, powder, lyophilized, for solution | 2 | 16.7% |
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.