Data / Drug companies / Abacavir
Abacavir: 8 companies and 9 products in the FDA NDC directory
Abacavir is listed in the FDA National Drug Code Directory by 8 companies, with 9 products in commercial distribution. 9 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; tablet, film coated; solution, and the newest product started marketing on May 28, 2021.
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- Companies listing it
- 8
- Products
- 9
- Generic (ANDA) products
- 9 (100.0%)
- Application numbers
- 4
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list abacavir
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Camber Pharmaceuticals, Inc. | 2 | tablet; solution | Generic drugs (ANDA) | April 1, 2021 |
| American Health Packaging | 1 | tablet, film coated | Generic drugs (ANDA) | February 4, 2013 |
| Aurobindo Pharma Limited | 1 | tablet, film coated | Generic drugs (ANDA) | December 17, 2012 |
| AvPAK | 1 | tablet | Generic drugs (ANDA) | April 10, 2020 |
| Cipla USA Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | November 21, 2017 |
| Coupler LLC | 1 | tablet | Generic drugs (ANDA) | April 1, 2021 |
| Major Pharmaceuticals | 1 | tablet, film coated | Generic drugs (ANDA) | December 17, 2012 |
| XLCare Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | May 28, 2021 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 4 | 44.4% |
| Tablet, film coated | 4 | 44.4% |
| Solution | 1 | 11.1% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 9 | 100% |
Pharmacologic classes
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.