Data / Drug companies / Naproxen sodium, pseudoephedrine hcl
Naproxen sodium, pseudoephedrine hcl: 4 companies and 4 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Naproxen sodium, pseudoephedrine hcl is listed in the FDA National Drug Code Directory by 4 companies, with 4 products in commercial distribution. 4 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, extended release, and the newest product started marketing on May 19, 2022.
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- Companies listing it
- 4
- Products
- 4
- Generic (ANDA) products
- 4 (100.0%)
- Application numbers
- 1
- Routes
- Oral
- Brand names
- Leader All Day Sinus and Cold D, Topcare Sinus and Cold D, All Day Sinus and Cold D, Sinus and Cold D
- openFDA record search
- api.fda.gov
Companies that list naproxen sodium, pseudoephedrine hcl
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Cardinal Health 110, LLC. DBA Leader | 1 | tablet, film coated, extended release | Generic drugs (ANDA) | May 19, 2022 |
| Meijer Distribution Inc | 1 | tablet, film coated, extended release | Generic drugs (ANDA) | August 12, 2013 |
| Topco Associates LLC | 1 | tablet, film coated, extended release | Generic drugs (ANDA) | August 14, 2013 |
| Walgreen Company | 1 | tablet, film coated, extended release | Generic drugs (ANDA) | May 23, 2013 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated, extended release | 4 | 100% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 4 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Nonsteroidal Anti-inflammatory Drug | 4 |
| alpha-Adrenergic Agonist | 4 |
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.