Data / Drug companies / Galantamine
Galantamine: 8 companies and 21 products in the FDA NDC directory
Galantamine is listed in the FDA National Drug Code Directory by 8 companies, with 21 products in commercial distribution. 21 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; capsule, extended release, and the newest product started marketing on March 6, 2024.
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- Companies listing it
- 8
- Products
- 21
- Generic (ANDA) products
- 21 (100.0%)
- Application numbers
- 3
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list galantamine
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Aurobindo Pharma Limited | 6 | capsule, extended release; tablet, film coated | Generic drugs (ANDA) | August 5, 2016 |
| Golden State Medical Supply, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | February 6, 2009 |
| Rising Pharma Holdings, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | March 29, 2011 |
| Slate Run Pharmaceuticals, LLC | 3 | tablet, film coated | Generic drugs (ANDA) | August 2, 2017 |
| Upsher-Smith Laboratories, LLC | 3 | tablet, film coated | Generic drugs (ANDA) | March 6, 2024 |
| American Health Packaging | 1 | tablet, film coated | Generic drugs (ANDA) | July 3, 2014 |
| Bryant Ranch Prepack | 1 | tablet, film coated | Generic drugs (ANDA) | March 29, 2011 |
| Bryant Ranch Prepack | 1 | tablet, film coated | Generic drugs (ANDA) | March 29, 2011 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 18 | 85.7% |
| Capsule, extended release | 3 | 14.3% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 21 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Cholinesterase Inhibitor | 21 |
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.