Data / Drug companies / Acetaminophen, dextromethorphan, phenylephrine
Acetaminophen, dextromethorphan, phenylephrine: 3 companies and 4 products in the FDA NDC directory
Acetaminophen, dextromethorphan, phenylephrine is listed in the FDA National Drug Code Directory by 3 companies, with 4 products in commercial distribution. 0 of the products (0.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are powder, for solution; capsule, liquid filled, and the newest product started marketing on August 8, 2025.
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- Companies listing it
- 3
- Products
- 4
- Generic (ANDA) products
- 0 (0.0%)
- Application numbers
- 1
- Routes
- Oral
- Brand names
- Sanatos Daytime, Theraflu PowerPods Daytime Severe Cold, Theraflu Daytime Severe Cold and Cough, Severe Cold and Cough Daytime
- openFDA record search
- api.fda.gov
Companies that list acetaminophen, dextromethorphan, phenylephrine
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Haleon US Holdings LLC | 2 | powder, for solution | Over the counter monograph drugs | July 28, 2018 |
| Pharmadel LLC | 1 | capsule, liquid filled | Over the counter monograph drugs | August 8, 2025 |
| WinCo Foods, LLC | 1 | powder, for solution | Over the counter monograph drugs | August 1, 2018 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Powder, for solution | 3 | 75% |
| Capsule, liquid filled | 1 | 25% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Over the counter monograph drugs | 4 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Sigma-1 Agonist | 4 |
| Uncompetitive N-methyl-D-aspartate Receptor Antagonist | 4 |
| alpha-1 Adrenergic Agonist | 4 |
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.