Data / Drug companies / Raltegravir
Raltegravir: 6 companies and 10 products in the FDA NDC directory
Raltegravir is listed in the FDA National Drug Code Directory by 6 companies, with 10 products in commercial distribution. 2 of the products (20.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet, chewable; granule, for suspension, and the newest product started marketing on October 14, 2026.
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- Companies listing it
- 6
- Products
- 10
- Generic (ANDA) products
- 2 (20.0%)
- Application numbers
- 5
- Routes
- Oral
- Brand names
- Isentress
- openFDA record search
- api.fda.gov
Companies that list raltegravir
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Merck Sharp & Dohme LLC | 5 | tablet, film coated; tablet, chewable | New drug applications (NDA) | May 26, 2017 |
| A-S Medication Solutions | 1 | tablet, film coated | New drug applications (NDA) | October 12, 2007 |
| Camber Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | December 19, 2024 |
| Lupin Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | October 14, 2026 |
| NuCare Pharmaceuticals,Inc. | 1 | tablet, film coated | New drug applications (NDA) | October 12, 2007 |
| Proficient Rx LP | 1 | tablet, film coated | New drug applications (NDA) | October 12, 2007 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 7 | 70% |
| Tablet, chewable | 2 | 20% |
| Granule, for suspension | 1 | 10% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| New drug applications (NDA) | 8 | 80% |
| Generic drugs (ANDA) | 2 | 20% |
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.