Data / Drug companies / Naproxen sodium, pseudoephedrine hydrochloride
Naproxen sodium, pseudoephedrine hydrochloride: 3 companies and 3 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Naproxen sodium, pseudoephedrine hydrochloride is listed in the FDA National Drug Code Directory by 3 companies, with 3 products in commercial distribution. 3 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, extended release; tablet, extended release, and the newest product started marketing on July 1, 2026.
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- Companies listing it
- 3
- Products
- 3
- Generic (ANDA) products
- 3 (100.0%)
- Application numbers
- 1
- Routes
- Oral
- Brand names
- Aleve-D Sinus and Headache, Sinus and Cold D, Mucinex DS 12HR Cold, Fever and Sinus
- openFDA record search
- api.fda.gov
Companies that list naproxen sodium, pseudoephedrine hydrochloride
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Bayer HealthCare LLC. | 1 | tablet | Generic drugs (ANDA) | January 1, 2014 |
| CVS Woonsocket Prescription Center, Incorporated | 1 | tablet, film coated, extended release | Generic drugs (ANDA) | May 8, 2024 |
| Reckitt Benckiser LLC | 1 | tablet, extended release | Generic drugs (ANDA) | July 1, 2026 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 1 | 33.3% |
| Tablet, film coated, extended release | 1 | 33.3% |
| Tablet, extended release | 1 | 33.3% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 3 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Nonsteroidal Anti-inflammatory Drug | 3 |
| alpha-Adrenergic Agonist | 3 |
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.