Data / Drug companies / Sulindac
Sulindac: 8 companies and 14 products in the FDA NDC directory
Sulindac is listed in the FDA National Drug Code Directory by 8 companies, with 14 products in commercial distribution. 14 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, and the newest product started marketing on November 14, 2016.
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- Companies listing it
- 8
- Products
- 14
- Generic (ANDA) products
- 14 (100.0%)
- Application numbers
- 6
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list sulindac
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| A-S Medication Solutions | 2 | tablet | Generic drugs (ANDA) | January 25, 2010 |
| Actavis Pharma, Inc. | 2 | tablet | Generic drugs (ANDA) | April 3, 1990 |
| Epic Pharma, LLC | 2 | tablet | Generic drugs (ANDA) | January 25, 2010 |
| PD-Rx Pharmaceuticals, Inc. | 2 | tablet | Generic drugs (ANDA) | September 4, 2009 |
| Puracap Laboratories LLC DBA Blu Pharmaceuticals | 2 | tablet | Generic drugs (ANDA) | November 14, 2016 |
| Sun Pharmaceutical Industries, Inc. | 2 | tablet | Generic drugs (ANDA) | September 4, 2009 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet | Generic drugs (ANDA) | April 3, 1990 |
| Proficient Rx LP | 1 | tablet | Generic drugs (ANDA) | January 25, 2010 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 14 | 100% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 14 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Nonsteroidal Anti-inflammatory Drug | 14 |
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.