Data / Drug companies / Nabumetone
Nabumetone: 30 companies and 64 products in the FDA NDC directory
Nabumetone is listed in the FDA National Drug Code Directory by 30 companies, with 64 products in commercial distribution. 64 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, and the newest product started marketing on January 7, 2025.
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- Companies listing it
- 30
- Products
- 64
- Generic (ANDA) products
- 64 (100.0%)
- Application numbers
- 7
- Routes
- Oral
- Brand names
- Relafen DS
- openFDA record search
- api.fda.gov
Companies that list nabumetone
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Bryant Ranch Prepack | 6 | tablet; tablet, film coated | Generic drugs (ANDA) | June 26, 2019 |
| Bryant Ranch Prepack | 4 | tablet | Generic drugs (ANDA) | June 26, 2019 |
| Proficient Rx LP | 4 | tablet; tablet, film coated | Generic drugs (ANDA) | September 25, 2019 |
| Advanced Rx of Tennessee, LLC | 3 | tablet; tablet, film coated | Generic drugs (ANDA) | June 26, 2019 |
| LGM Pharma Solutions, LLC | 3 | tablet, film coated | Generic drugs (ANDA) | September 4, 2019 |
| Northwind Health Company, LLC | 3 | tablet; tablet, film coated | Generic drugs (ANDA) | July 7, 2021 |
| A-S Medication Solutions | 2 | tablet | Generic drugs (ANDA) | June 26, 2019 |
| Actavis Pharma, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | June 13, 2011 |
| Ani Pharmaceuticals, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | January 7, 2025 |
| Bryant Ranch Prepack | 2 | tablet | Generic drugs (ANDA) | June 26, 2019 |
| Chartwell RX, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | February 25, 2002 |
| Cipla USA Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | March 6, 2019 |
| Direct_Rx | 2 | tablet | Generic drugs (ANDA) | May 11, 2021 |
| Exelan Pharmaceuticals Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | April 14, 2015 |
| Lupin Pharmaceuticals, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | January 12, 2011 |
| PD-Rx Pharmaceuticals, Inc. | 2 | tablet | Generic drugs (ANDA) | June 26, 2019 |
| Preferred Pharmaceuticals Inc. | 2 | tablet | Generic drugs (ANDA) | July 15, 2020 |
| Quality Care Products, LLC | 2 | tablet | Generic drugs (ANDA) | February 28, 2020 |
| Remedyrepack Inc. | 2 | tablet | Generic drugs (ANDA) | April 7, 2024 |
| ScieGen Pharmaceuticals, Inc. | 2 | tablet | Generic drugs (ANDA) | June 26, 2019 |
| Sportpharm LLC | 2 | tablet | Generic drugs (ANDA) | June 26, 2019 |
| St. Mary's Medical Park Pharmacy | 2 | tablet | Generic drugs (ANDA) | October 21, 2019 |
| Westminster Pharmaceuticals, LLC | 2 | tablet | Generic drugs (ANDA) | September 25, 2019 |
| American Health Packaging | 1 | tablet, film coated | Generic drugs (ANDA) | March 23, 2022 |
| Asclemed USA Inc. | 1 | tablet | Generic drugs (ANDA) | June 26, 2019 |
| Asclemed USA, Inc. | 1 | tablet | Generic drugs (ANDA) | June 26, 2019 |
| Carwin Pharmaceutical Associates, LLC | 1 | tablet | Generic drugs (ANDA) | September 20, 2019 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | March 6, 2019 |
| Proficient Rx LP | 1 | tablet, film coated | Generic drugs (ANDA) | June 13, 2011 |
| Redpharm Drug | 1 | tablet | Generic drugs (ANDA) | June 26, 2019 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 41 | 64.1% |
| Tablet, film coated | 23 | 35.9% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 64 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Nonsteroidal Anti-inflammatory Drug | 64 |
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.