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Data / Drug companies / Acetaminophen, chlorpheniramine maleate

Acetaminophen, chlorpheniramine maleate: 5 companies and 5 products in the FDA NDC directory

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

Acetaminophen, chlorpheniramine maleate is listed in the FDA National Drug Code Directory by 5 companies, with 5 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 tablet, film coated; liquid, and the newest product started marketing on January 23, 2023.

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Companies listing it
5
Products
5
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Oral
Brand names
Cold and Flu HBP, Cold and Flu HBP, Nocold-S
openFDA record search
api.fda.gov

Companies that list acetaminophen, chlorpheniramine maleate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
CVS Pharmacy1tablet, film coatedOver the counter monograph drugsJuly 16, 2017
Kroger Company1tablet, film coatedOver the counter monograph drugsApril 14, 2022
Lydia Co., Ltd.1liquidOther unapproved drugsJanuary 23, 2023
Meijer Distribution Inc1tablet, film coatedOver the counter monograph drugsJuly 16, 2017
Walmart Inc.1tablet, film coatedOver the counter monograph drugsApril 14, 2022

Dosage forms

Dosage formProductsShare
Tablet, film coated480%
Liquid120%

Marketing categories

Marketing categoryProductsShare
Over the counter monograph drugs480%
Other unapproved drugs120%

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.