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Data / Drug companies / Acetaminophen and dextromethorphan hydrobromide

Acetaminophen and dextromethorphan hydrobromide: 6 companies and 9 products in the FDA NDC directory

Acetaminophen and dextromethorphan hydrobromide is listed in the FDA National Drug Code Directory by 6 companies, with 9 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 suspension; tablet, film coated; liquid, and the newest product started marketing on June 18, 2026.

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Companies listing it
6
Products
9
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Oral
Brand names
Extra Strength Tylenol Cold Plus Flu Multi Symptom Day, Extra Strength Tylenol Severe Cough Plus Sore Throat Day, Childrens Tylenol Cold Plus Cough Plus Sore Throat, Daytime Cold and Flu, Delsym Cough Plus Sore Throat, Mucinex Childrens Mighty Chews Cold and Flu, Extra Strength Tylenol Severe Cough Plus Sore Throat Day, CVS Childrens Cold Plus Cough Plus Sore Throat
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Companies that list acetaminophen and dextromethorphan hydrobromide

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Kenvue Brands LLC4tablet, film coated; liquidOver the counter monograph drugsJune 18, 2026
CVS Woonsocket Prescription Center, Incorporated1suspensionOver the counter monograph drugsFebruary 1, 2023
Humanwell PuraCap Pharmaceutical (Wuhan), Ltd.1capsule, liquid filledOver the counter monograph drugsDecember 28, 2025
Reckitt Benckiser LLC1solutionOver the counter monograph drugsJuly 1, 2019
Reckitt Benckiser LLC1tablet, chewableOver the counter monograph drugsJune 1, 2025
Walgreen Company1suspensionOver the counter monograph drugsFebruary 24, 2023

Dosage forms

Dosage formProductsShare
Suspension333.3%
Tablet, film coated222.2%
Liquid111.1%
Capsule, liquid filled111.1%
Solution111.1%
Tablet, chewable111.1%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs9100%

Pharmacologic classes

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.