Data / Drug companies / Naproxen sodium 220mg
Naproxen sodium 220mg: 5 companies and 5 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Naproxen sodium 220mg is listed in the FDA National Drug Code Directory by 5 companies, with 5 products in commercial distribution. 5 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, coated; tablet, film coated; tablet, and the newest product started marketing on March 18, 2026.
The request: Get every company that lists naproxen sodium 220mg in the FDA NDC directory, with headquarters, website and number of employees. $10 of work on sign-up, no card.
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- Companies listing it
- 5
- Products
- 5
- Generic (ANDA) products
- 5 (100.0%)
- Application numbers
- 1
- Routes
- Oral
- Brand names
- Naproxen Sodium
- openFDA record search
- api.fda.gov
Companies that list naproxen sodium 220mg
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Allegiant Health | 1 | tablet, coated | Generic drugs (ANDA) | May 4, 2011 |
| Athlete's Needs, Inc. | 1 | tablet, coated | Generic drugs (ANDA) | December 23, 2014 |
| CVS Woonsocket Prescription Center, Incorporated | 1 | tablet | Generic drugs (ANDA) | May 1, 2025 |
| Command Brands, LLC | 1 | tablet, coated | Generic drugs (ANDA) | December 23, 2014 |
| Grocery Outlet, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | March 18, 2026 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, coated | 3 | 60% |
| Tablet, film coated | 1 | 20% |
| Tablet | 1 | 20% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 5 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Nonsteroidal Anti-inflammatory Drug | 5 |
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.