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Data / Drug companies / Ketotifen fumarate

Ketotifen fumarate: 19 companies and 22 products in the FDA NDC directory

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

Ketotifen fumarate is listed in the FDA National Drug Code Directory by 19 companies, with 22 products in commercial distribution. 8 of the products (36.4%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are solution/ drops; solution, and the newest product started marketing on April 15, 2026.

The request: Get every company that lists ketotifen fumarate 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
19
Products
22
Generic (ANDA) products
8 (36.4%)
Application numbers
4
Routes
Ophthalmic
Brand names
Eye Itch Relief, Alaway, Equate Eye Itch Relief, Zaditor
openFDA record search
api.fda.gov

Companies that list ketotifen fumarate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions2solution/ dropsNew drug applications (NDA)April 1, 2024
Cardinal Health 110, LLC. DBA Leader2solution/ drops; solutionGeneric drugs (ANDA)August 7, 2020
Preferred Pharmaceuticals Inc.2solution/ drops; solutionGeneric drugs (ANDA)February 27, 2026
Alcon Laboratories, Inc.1solutionGeneric drugs (ANDA)January 8, 2013
Armas Pharmaceuticals Inc.1solution/ dropsGeneric drugs (ANDA)October 9, 2023
Bausch & Lomb Incorporated1solution/ dropsNew drug applications (NDA)December 1, 2006
CVS Pharmacy1solution/ dropsNew drug applications (NDA)April 1, 2020
Kroger Company1solution/ dropsNew drug applications (NDA)June 1, 2022
Perrigo Direct, Inc1solution/ dropsNew drug applications (NDA)April 1, 2024
Proficient Rx LP1solution/ dropsGeneric drugs (ANDA)October 1, 2007
Redpharm Drug1solutionNew drug applications (NDA)August 7, 2020
Rugby Laboratories1solution/ dropsAuthorized generics (NDA)September 18, 2020
Safeway1solutionNew drug applications (NDA)August 20, 2014
Sentiss Pharmaceuticals LLC1solution/ dropsGeneric drugs (ANDA)April 15, 2026
Target Corporation1solutionNew drug applications (NDA)January 2, 2014
Topco Associates LLC1solution/ dropsNew drug applications (NDA)March 15, 2022
Unichem Pharmaceuticals (USA), Inc.1solutionGeneric drugs (ANDA)October 15, 2021
Wal-Mart Stores Inc1solutionNew drug applications (NDA)January 1, 2016
Walgreen Company1solutionNew drug applications (NDA)September 3, 2013

Dosage forms

Dosage formProductsShare
Solution/ drops1359.1%
Solution940.9%

Marketing categories

Marketing categoryProductsShare
New drug applications (NDA)1254.5%
Generic drugs (ANDA)836.4%
Authorized generics (NDA)29.1%

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.