Data / Drug companies / Ergot Derivative
Ergot Derivative drugs: 4 drugs from 29 companies in the FDA NDC directory
Ergot Derivative is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 37 products in this class from 29 companies, covering 4 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on August 1, 2026.
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- 29Companies
- 37Products
- 4Drugs by generic name
Drugs in the Ergot Derivative class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Methylergonovine maleate | 14 | 13 |
| Cabergoline | 12 | 9 |
| Bromocriptine mesylate | 10 | 9 |
| Methylergonovine | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| A-S Medication Solutions | 4 | tablet | Generic drugs (ANDA) | October 3, 2024 |
| American Health Packaging | 2 | tablet | Generic drugs (ANDA) | June 12, 2026 |
| Amneal Pharmaceuticals NY LLC | 2 | tablet | Generic drugs (ANDA) | October 3, 2024 |
| Ani Pharmaceuticals, Inc. | 2 | tablet; capsule | New drug applications (NDA) | April 6, 2026 |
| HF Acquisition Co LLC, DBA HealthFirst | 2 | injection; injection, solution | Generic drugs (ANDA) | June 14, 2021 |
| Teva Pharmaceuticals USA, Inc. | 2 | tablet | Generic drugs (ANDA) | March 26, 2019 |
| American Regent, Inc. | 1 | injection, solution | Generic drugs (ANDA) | June 21, 2010 |
| Avvisto Therapeutics LLC | 1 | tablet | New drug applications (NDA) | May 23, 2024 |
| Breckenridge Pharmaceutical, Inc. | 1 | injection | Generic drugs (ANDA) | November 7, 2016 |
| Bryant Ranch Prepack | 1 | injection | Generic drugs (ANDA) | November 7, 2016 |
| Bryant Ranch Prepack | 1 | injection | Generic drugs (ANDA) | November 7, 2016 |
| Cranbury Pharmaceuticals, LLC | 1 | tablet | Generic drugs (ANDA) | August 1, 2026 |
| Granules Pharmaceuticals Inc. | 1 | tablet | Generic drugs (ANDA) | May 25, 2018 |
| Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc. | 1 | tablet | Generic drugs (ANDA) | June 15, 2022 |
| Ingenus Pharmaceuticals, LLC | 1 | tablet | Generic drugs (ANDA) | August 9, 2018 |
| Lupin Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | April 4, 2016 |
| Major Pharmaceuticals | 1 | tablet | Generic drugs (ANDA) | September 13, 2024 |
| Mylan Pharmaceuticals Inc. | 1 | tablet | Authorized generics (NDA) | September 22, 2014 |
| Mylan Pharmaceuticals Inc. | 1 | capsule | Generic drugs (ANDA) | June 17, 2013 |
| Padagis US LLC | 1 | tablet | Generic drugs (ANDA) | April 1, 2014 |
| Pharmacist Pharmaceutical, LLC | 1 | injection, solution | Generic drugs (ANDA) | November 1, 2010 |
| Remedyrepack Inc. | 1 | tablet | Generic drugs (ANDA) | April 24, 2026 |
| Rising Pharma Holdings, Inc. | 1 | tablet | Generic drugs (ANDA) | January 15, 2021 |
| Sandoz Inc | 1 | tablet | Generic drugs (ANDA) | January 13, 1998 |
| Sola Pharmaceuticals, LLC | 1 | tablet | Generic drugs (ANDA) | May 8, 2023 |
| Somerset Therapeutics, LLC | 1 | tablet | Generic drugs (ANDA) | October 18, 2024 |
| Volley Pharmaceuticals, LLC | 1 | tablet | Generic drugs (ANDA) | March 15, 2024 |
| Zydus Lifesciences Limited | 1 | capsule | Generic drugs (ANDA) | January 23, 2009 |
| Zydus Pharmaceuticals USA Inc. | 1 | capsule | Generic drugs (ANDA) | January 23, 2009 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 26 | 70.3% |
| Injection | 4 | 10.8% |
| Capsule | 4 | 10.8% |
| Injection, solution | 3 | 8.1% |
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.