Data / Drug companies / Acetaminophen, dextromethorphan hbr
Acetaminophen, dextromethorphan hbr: 20 companies and 35 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Acetaminophen, dextromethorphan hbr is listed in the FDA National Drug Code Directory by 20 companies, with 35 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; liquid; solution, and the newest product started marketing on July 7, 2026.
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- Companies listing it
- 20
- Products
- 35
- Generic (ANDA) products
- 0 (0.0%)
- Application numbers
- 2
- Routes
- Oral
- Brand names
- Theraflu Severe Cold Relief Daytime, Daytime Cold and Flu, Theraflu Flu Relief Max Strength Daytime, Mucinex Childrens Multi-Symptom Cold and Flu, Daytime Severe Cold and Flu, Vicks DayQuil and Vicks NyQuil Intense Flu, Good Neighbor Pharmacy Daytime Flu Relief Max Strength, Pain, Headache and Cough
- openFDA record search
- api.fda.gov
Companies that list acetaminophen, dextromethorphan hbr
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 | 6 | powder, for solution; syrup | Over the counter monograph drugs | June 19, 2024 |
| CVS Woonsocket Prescription Center, Incorporated | 5 | tablet, film coated; capsule, liquid filled | Over the counter monograph drugs | April 21, 2026 |
| The Procter & Gamble Manufacturing Company | 5 | liquid; kit | Over the counter monograph drugs | July 7, 2026 |
| Genexa Inc. | 2 | suspension | Over the counter monograph drugs | July 31, 2025 |
| The Procter & Gamble Manufacturing Company | 2 | liquid; capsule, liquid filled | Over the counter monograph drugs | July 9, 2024 |
| Amerisource Bergen | 1 | powder, for solution | Over the counter monograph drugs | May 4, 2026 |
| CVS Pharmacy | 1 | solution | Over the counter monograph drugs | April 15, 2019 |
| Cardinal Health 110, LLC. DBA Leader | 1 | powder, for solution | Over the counter monograph drugs | July 1, 2026 |
| Haleon US Holdings LLC | 1 | solution | Over the counter monograph drugs | June 15, 2020 |
| Haleon US Holdings LLC | 1 | tablet | Over the counter monograph drugs | April 30, 2026 |
| Kroger Company | 1 | tablet, film coated | Over the counter monograph drugs | August 4, 2025 |
| Nuvicare LLC | 1 | capsule, liquid filled | Over the counter monograph drugs | June 17, 2026 |
| Pharmadel LLC | 1 | liquid | Over the counter monograph drugs | December 1, 2023 |
| Procter & Gamble Manufactura S de RL de CV | 1 | powder, for solution | Over the counter monograph drugs | June 11, 2025 |
| R J General Corporation | 1 | powder, for solution | Over the counter monograph drugs | November 12, 2024 |
| Raritan Pharmaceuticals Inc | 1 | solution | Over the counter monograph drugs | April 24, 2023 |
| Reckitt Benckiser LLC | 1 | solution | Over the counter monograph drugs | June 1, 2026 |
| Select Consumer Group | 1 | powder, for solution | Over the counter monograph drugs | December 1, 2023 |
| Walgreen Company | 1 | powder, for solution | Over the counter monograph drugs | March 7, 2025 |
| Walmart Inc. | 1 | tablet, film coated | Over the counter monograph drugs | May 14, 2026 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Powder, for solution | 10 | 28.6% |
| Liquid | 7 | 20% |
| Solution | 5 | 14.3% |
| Tablet, film coated | 3 | 8.6% |
| Capsule, liquid filled | 3 | 8.6% |
| Suspension | 2 | 5.7% |
| Kit | 1 | 2.9% |
| Syrup | 1 | 2.9% |
| Powder | 1 | 2.9% |
| Tablet | 1 | 2.9% |
| Tablet, chewable | 1 | 2.9% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Over the counter monograph drugs | 35 | 100% |
Pharmacologic classes
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.