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Data / Drug companies / Pseudoephedrine hydrochloride

Pseudoephedrine hydrochloride: 23 companies and 39 products in the FDA NDC directory

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

Pseudoephedrine hydrochloride is listed in the FDA National Drug Code Directory by 23 companies, with 39 products in commercial distribution. 30 of the products (76.9%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated, extended release; tablet, film coated; tablet, and the newest product started marketing on January 30, 2026.

The request: Get every company that lists pseudoephedrine hydrochloride in the FDA NDC directory, with headquarters, website and number of employees. $10 of work on sign-up, no card.

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Companies listing it
23
Products
39
Generic (ANDA) products
30 (76.9%)
Application numbers
4
Routes
Oral
Brand names
Nasal Decongestant, 12 Hour Nasal Decongestant, Sudafed Sinus Congestion 12 Hour, Leader 12 Hour Nasal Decongestant, Sinus and Nasal Decongestant, Zephrex D, Good Neighbor Pharmacy Nasal Decongestant, Nasal Decongestant D
openFDA record search
api.fda.gov

Companies that list pseudoephedrine hydrochloride

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Major Pharmaceuticals4tablet; tablet, film coatedOver the counter monograph drugsJune 7, 2024
A-S Medication Solutions3tablet, film coated, extended release; tabletGeneric drugs (ANDA)August 26, 2019
Cardinal Health 110, LLC. DBA Leader3tablet, film coated, extended release; tabletGeneric drugs (ANDA)May 16, 2024
Kenvue Brands LLC3solution; tablet, film coated, extended releaseOver the counter monograph drugsJuly 31, 2021
Walgreen Company3tablet, film coated, extended release; tablet, extended releaseGeneric drugs (ANDA)January 30, 2026
CVS Woonsocket Prescription Center, Incorporated2tablet, film coated, extended release; tablet, film coatedGeneric drugs (ANDA)January 20, 2026
Kroger Company2tablet, film coated; tabletOver the counter monograph drugsFebruary 19, 2021
L. Perrigo Company2capsule, gelatin coated; tablet, film coated, extended releaseOver the counter monograph drugsNovember 4, 2016
Ohm Laboratories Inc.2tablet, extended release; tablet, film coatedGeneric drugs (ANDA)April 28, 2006
Publix Super Markets Inc2tablet, film coated, extended releaseGeneric drugs (ANDA)April 28, 2006
Amerisource Bergen1tablet, film coated, extended releaseGeneric drugs (ANDA)August 12, 1999
Aurohealth LLC1tablet, extended releaseGeneric drugs (ANDA)December 29, 2025
CVS Pharmacy1tablet, film coated, extended releaseGeneric drugs (ANDA)December 1, 1999
Chain Drug Marketing Association1tablet, film coated, extended releaseGeneric drugs (ANDA)April 28, 2006
H E B1tablet, extended releaseGeneric drugs (ANDA)May 15, 2019
HyVee Inc1tablet, film coated, extended releaseGeneric drugs (ANDA)September 11, 2000
Meijer Distribution Inc1tablet, film coated, extended releaseGeneric drugs (ANDA)November 28, 2018
Sam's West Inc1tablet, film coatedGeneric drugs (ANDA)February 7, 2012
Sportpharm LLC1tablet, film coatedGeneric drugs (ANDA)April 28, 2006
Strategic Sourcing Services LLC1tablet, film coatedGeneric drugs (ANDA)August 10, 2023
Topco Associates LLC1tablet, film coated, extended releaseGeneric drugs (ANDA)April 25, 2000
United Natural Foods, Inc. DBA Unfi1tablet, film coated, extended releaseGeneric drugs (ANDA)August 10, 2004
Wal-Mart Stores Inc1tablet, film coated, extended releaseGeneric drugs (ANDA)June 24, 2020

Dosage forms

Dosage formProductsShare
Tablet, film coated, extended release1743.6%
Tablet, film coated1025.6%
Tablet615.4%
Tablet, extended release410.3%
Capsule, gelatin coated12.6%
Solution12.6%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)3076.9%
Over the counter monograph drugs923.1%

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.