Data / Drug companies / Dextromethorphan hbr, guaifenesin, chlorpheniramine maleate
Dextromethorphan hbr, guaifenesin, chlorpheniramine maleate: 3 companies and 4 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Dextromethorphan hbr, guaifenesin, chlorpheniramine maleate 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 kit, and the newest product started marketing on August 20, 2026.
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- Companies listing it
- 3
- Products
- 4
- Generic (ANDA) products
- 0 (0.0%)
- Application numbers
- 1
- Routes
- Oral
- Brand names
- Kids Daytime Cough and Nighttime Cough Combo Pack, Walgreens Day and Night Pack, Daytime and Nighttime Cough and Chest Congestion Childrens
- openFDA record search
- api.fda.gov
Companies that list dextromethorphan hbr, guaifenesin, chlorpheniramine maleate
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Genexa Inc. | 2 | kit | Over the counter monograph drugs | August 20, 2026 |
| CVS Pharmacy | 1 | kit | Over the counter monograph drugs | February 19, 2019 |
| Walgreen Company | 1 | kit | Over the counter monograph drugs | April 13, 2020 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Kit | 4 | 100% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Over the counter monograph drugs | 4 | 100% |
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.