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Data / Drug companies / Guaifenesin, pseudoephedrine hydrochloride

Guaifenesin, pseudoephedrine hydrochloride: 8 companies and 8 products in the FDA NDC directory

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

Guaifenesin, pseudoephedrine hydrochloride is listed in the FDA National Drug Code Directory by 8 companies, with 8 products in commercial distribution. 8 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, multilayer, extended release, and the newest product started marketing on April 2, 2026.

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Companies listing it
8
Products
8
Generic (ANDA) products
8 (100.0%)
Application numbers
1
Routes
Oral
Brand names
Mucus Relief D, Mucus D, Mucus D, Leader Mucus Relief D, Foster and Thrive Mucus Relief D, Nasal and Chest Decongestant, Equate Mucus D
openFDA record search
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Companies that list guaifenesin, pseudoephedrine hydrochloride

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
CVS Woonsocket Prescription Center, Incorporated1tablet, multilayer, extended releaseGeneric drugs (ANDA)April 4, 2025
Cardinal Health 110, LLC. DBA Leader1tablet, multilayer, extended releaseGeneric drugs (ANDA)March 8, 2025
H E B1tablet, multilayer, extended releaseGeneric drugs (ANDA)November 30, 2023
L. Perrigo Company1tablet, multilayer, extended releaseGeneric drugs (ANDA)October 3, 2025
Publix Super Markets Inc1tablet, multilayer, extended releaseGeneric drugs (ANDA)April 2, 2026
Strategic Sourcing Services LLC1tablet, multilayer, extended releaseGeneric drugs (ANDA)November 20, 2024
Walgreen Company1tablet, multilayer, extended releaseGeneric drugs (ANDA)March 26, 2024
Walmart Inc.1tablet, multilayer, extended releaseGeneric drugs (ANDA)December 5, 2025

Dosage forms

Dosage formProductsShare
Tablet, multilayer, extended release8100%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)8100%

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.