Data / Drug companies / Abacavir and lamivudine
Abacavir and lamivudine: 6 companies and 6 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Abacavir and lamivudine is listed in the FDA National Drug Code Directory by 6 companies, with 6 products in commercial distribution. 6 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, and the newest product started marketing on April 16, 2025.
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- Companies listing it
- 6
- Products
- 6
- Generic (ANDA) products
- 6 (100.0%)
- Application numbers
- 6
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list abacavir and lamivudine
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Aurobindo Pharma Limited | 1 | tablet, film coated | Generic drugs (ANDA) | November 15, 2018 |
| Camber Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | April 16, 2025 |
| Cipla USA Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | March 28, 2017 |
| Laurus Labs Limited | 1 | tablet, film coated | Generic drugs (ANDA) | July 25, 2022 |
| Lupin Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | March 28, 2017 |
| Macleods Pharmaceuticals Limited | 1 | tablet, film coated | Generic drugs (ANDA) | December 20, 2024 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 6 | 100% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 6 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor | 6 |
| Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor | 6 |
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.