Data / Drug companies / Dopaminergic Agonist
Dopaminergic Agonist drugs: 1 drug from 5 companies in the FDA NDC directory
Dopaminergic Agonist is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 6 products in this class from 5 companies, covering 1 drug by generic name. The main marketing category is unapproved homeopathic products, and the newest product started marketing on February 4, 2025.
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.
- 5Companies
- 6Products
- 1Drugs by generic name
Drugs in the Dopaminergic Agonist class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Apomorphine hydrochloride | 3 | 2 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| MDD US Operations LLC, a Subsidiary of Supernus Pharmaceuticals, Inc. | 2 | injection; injection, solution | New drug applications (NDA) | February 4, 2025 |
| Dna Labs, Inc. | 1 | solution | Unapproved homeopathic products | January 1, 1990 |
| Guna Spa | 1 | solution/ drops | Unapproved homeopathic products | May 12, 2010 |
| Professional Complementary Health Formulas | 1 | liquid | Unapproved homeopathic products | August 15, 1984 |
| TruPharma, LLC | 1 | injection | Generic drugs (ANDA) | February 24, 2022 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection | 2 | 33.3% |
| Injection, solution | 1 | 16.7% |
| Solution | 1 | 16.7% |
| Solution/ drops | 1 | 16.7% |
| Liquid | 1 | 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.