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Data / Drug companies / Fexofenadine hydrochloride and pseudoephedrine hydrochloride

Fexofenadine hydrochloride and pseudoephedrine hydrochloride: 16 companies and 24 products in the FDA NDC directory

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

Fexofenadine hydrochloride and pseudoephedrine hydrochloride is listed in the FDA National Drug Code Directory by 16 companies, with 24 products in commercial distribution. 21 of the products (87.5%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated, extended release; tablet, extended release, and the newest product started marketing on August 27, 2026.

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Companies listing it
16
Products
24
Generic (ANDA) products
21 (87.5%)
Application numbers
6
Routes
Oral
Brand names
Allegra-D Allergy and Congestion, 12HR Allergy & Congestion Relief, Allegra-D
openFDA record search
api.fda.gov

Companies that list fexofenadine hydrochloride and pseudoephedrine hydrochloride

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Walgreen Company4tablet, film coated, extended release; tablet, extended releaseGeneric drugs (ANDA)August 27, 2026
Aurohealth LLC2tablet, film coated, extended releaseGeneric drugs (ANDA)April 17, 2025
CVS Pharmacy2tablet, extended release; tablet, film coated, extended releaseGeneric drugs (ANDA)August 27, 2020
CVS Woonsocket Prescription Center, Incorporated2tablet, extended release; tablet, film coated, extended releaseGeneric drugs (ANDA)November 17, 2022
Chattem, Inc.2tablet, film coated, extended releaseNew drug applications (NDA)March 3, 2011
Kroger Company2tablet, film coated, extended release; tablet, extended releaseGeneric drugs (ANDA)March 31, 2022
A-S Medication Solutions1tablet, film coated, extended releaseNew drug applications (NDA)March 3, 2011
Amerisource Bergen1tablet, film coated, extended releaseGeneric drugs (ANDA)March 1, 2018
Cardinal Health 110, LLC. DBA Leader1tablet, film coated, extended releaseGeneric drugs (ANDA)May 15, 2024
H E B1tablet, film coated, extended releaseGeneric drugs (ANDA)August 1, 2018
Ohm Laboratories Inc.1tablet, film coated, extended releaseGeneric drugs (ANDA)March 1, 2018
Publix Super Markets, Inc1tablet, extended releaseGeneric drugs (ANDA)November 8, 2021
Rite Aid Corporation1tablet, extended releaseGeneric drugs (ANDA)March 31, 2022
Strategic Sourcing Services LLC1tablet, extended releaseGeneric drugs (ANDA)March 31, 2022
Sun Pharmaceutical Industries, Inc.1tablet, film coated, extended releaseGeneric drugs (ANDA)March 1, 2018
Walmart Inc.1tablet, extended releaseGeneric drugs (ANDA)March 31, 2022

Dosage forms

Dosage formProductsShare
Tablet, film coated, extended release1666.7%
Tablet, extended release833.3%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)2187.5%
New drug applications (NDA)312.5%

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.