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Data / Drug companies / Acetaminophen, dextromethorphan hydrobromide, guaifenesin

Acetaminophen, dextromethorphan hydrobromide, guaifenesin: 7 companies and 8 products in the FDA NDC directory

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Acetaminophen, dextromethorphan hydrobromide, guaifenesin is listed in the FDA National Drug Code Directory by 7 companies, with 8 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 solution; liquid, and the newest product started marketing on July 1, 2026.

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Companies listing it
7
Products
8
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Oral
Brand names
Topcare Tussin CF Max, Tussin Severe, Severe Cough Cold and Flu, Good Sense Tussin, Robitussin Maximum Strength Severe Multi-Symptom Cough Cold Flu, Leader Tussin CF, CVS Pharmacy MS Adult Severe Multi Symptom Cough Cold Flu, Tussin CF Severe
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Companies that list acetaminophen, dextromethorphan hydrobromide, guaifenesin

Ranked by number of products. Finished drugs in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
CVS Woonsocket Prescription Center, Incorporated2solution; liquidOver the counter monograph drugsAugust 29, 2025
Amazon.com Services LLC1solutionOver the counter monograph drugsJuly 1, 2026
Cardinal Health 110, LLC. DBA Leader1solutionOver the counter monograph drugsSeptember 30, 2025
Haleon US Holdings LLC1liquidOver the counter monograph drugsFebruary 15, 2024
HyVee Inc1solutionOver the counter monograph drugsJanuary 28, 2026
L. Perrigo Company1solutionOver the counter monograph drugsJanuary 8, 2026
Topco Associates LLC1solutionOver the counter monograph drugsFebruary 11, 2026

Dosage forms

Dosage formProductsShare
Solution675%
Liquid225%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs8100%

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.