Data / Drug companies / Etodolac
Etodolac: 31 companies and 104 products in the FDA NDC directory
Etodolac is listed in the FDA National Drug Code Directory by 31 companies, with 104 products in commercial distribution. 104 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; tablet, film coated, extended release, and the newest product started marketing on July 15, 2026.
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- Companies listing it
- 31
- Products
- 104
- Generic (ANDA) products
- 104 (100.0%)
- Application numbers
- 14
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list etodolac
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 | 9 | tablet, film coated; capsule | Generic drugs (ANDA) | February 13, 2026 |
| Bryant Ranch Prepack | 7 | tablet, film coated; capsule | Generic drugs (ANDA) | August 1, 2021 |
| Sun Pharmaceutical Industries, Inc. | 7 | tablet, extended release; tablet, film coated | Generic drugs (ANDA) | March 13, 2003 |
| Advanced Rx of Tennessee, LLC | 6 | tablet, film coated; tablet, extended release | Generic drugs (ANDA) | August 29, 2025 |
| Aphena Pharma Solutions - Tennessee, LLC | 6 | tablet, film coated | Generic drugs (ANDA) | June 11, 2018 |
| Golden State Medical Supply, Inc. | 6 | tablet, extended release; tablet, film coated | Generic drugs (ANDA) | March 13, 2003 |
| Bryant Ranch Prepack | 5 | capsule; tablet, film coated, extended release | Generic drugs (ANDA) | March 9, 2015 |
| Apotex Corp. | 4 | tablet, film coated; capsule | Generic drugs (ANDA) | May 1, 2003 |
| Ipca Laboratories Limited | 4 | capsule; tablet | Generic drugs (ANDA) | February 13, 2026 |
| NorthStar Rx LLC | 3 | tablet, extended release | Generic drugs (ANDA) | March 13, 2003 |
| Northwind Health Company, LLC | 3 | tablet, film coated; capsule | Generic drugs (ANDA) | July 8, 2021 |
| PD-Rx Pharmaceuticals, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | May 1, 2003 |
| Preferred Pharmaceuticals Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | March 24, 2025 |
| Proficient Rx LP | 3 | tablet, film coated; tablet, film coated, extended release | Generic drugs (ANDA) | March 9, 2015 |
| Proficient Rx LP | 3 | tablet, film coated, extended release; tablet, extended release | Generic drugs (ANDA) | February 15, 2014 |
| Remedyrepack Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | December 30, 2025 |
| Teva Pharmaceuticals USA, Inc. | 3 | tablet, film coated, extended release | Generic drugs (ANDA) | February 9, 2001 |
| Zydus Lifesciences Limited | 3 | tablet, film coated, extended release | Generic drugs (ANDA) | February 15, 2014 |
| Zydus Pharmaceuticals USA Inc. | 3 | tablet, film coated, extended release | Generic drugs (ANDA) | February 15, 2014 |
| Amneal Pharmaceuticals NY LLC | 2 | tablet, film coated | Generic drugs (ANDA) | June 11, 2018 |
| Ani Pharmaceuticals, Inc. | 2 | capsule | Generic drugs (ANDA) | March 9, 2015 |
| Aurobindo Pharma Limited | 2 | tablet, film coated | Generic drugs (ANDA) | July 15, 2026 |
| Bryant Ranch Prepack | 2 | capsule | Generic drugs (ANDA) | March 9, 2015 |
| Chartwell RX, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | December 7, 2018 |
| Edenbridge Pharmaceuticals LLC. | 2 | tablet, film coated | Generic drugs (ANDA) | December 7, 2018 |
| St. Mary's Medical Park Pharmacy | 2 | tablet, film coated, extended release; tablet, film coated | Generic drugs (ANDA) | March 14, 2018 |
| Unichem Pharmaceuticals (USA), Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | August 1, 2021 |
| Doc Rx | 1 | tablet, film coated | Generic drugs (ANDA) | June 11, 2018 |
| Medsource Pharmaceuticals | 1 | tablet, film coated | Generic drugs (ANDA) | May 1, 2003 |
| NuCare Pharmaceuticals,Inc. | 1 | tablet, film coated, extended release | Generic drugs (ANDA) | February 15, 2014 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | May 1, 2003 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 55 | 52.9% |
| Capsule | 20 | 19.2% |
| Tablet, film coated, extended release | 15 | 14.4% |
| Tablet, extended release | 11 | 10.6% |
| Tablet | 3 | 2.9% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 104 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Nonsteroidal Anti-inflammatory Drug | 104 |
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.