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Data / Drug companies / Formoterol fumarate dihydrate

Formoterol fumarate dihydrate: 6 companies and 6 products in the FDA NDC directory

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

Formoterol fumarate dihydrate is listed in the FDA National Drug Code Directory by 6 companies, with 6 products in commercial distribution. 4 of the products (66.7%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are solution, and the newest product started marketing on June 30, 2025.

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Companies listing it
6
Products
6
Generic (ANDA) products
4 (66.7%)
Application numbers
4
Routes
Respiratory (inhalation)
Brand names
Formoterol Fumarate, Perforomist, Formoterol Fumarate, Formoterol Fumarate Inhalation Solution
openFDA record search
api.fda.gov

Companies that list formoterol fumarate dihydrate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Devatis, Inc.1solutionGeneric drugs (ANDA)June 30, 2025
Lifestar Pharma LLC1solutionGeneric drugs (ANDA)March 22, 2023
Mylan Pharmaceuticals Inc.1solutionAuthorized generics (NDA)June 22, 2021
NorthStar RxLLC1solutionGeneric drugs (ANDA)July 1, 2024
Ritedose Pharmaceuticals, LLC1solutionGeneric drugs (ANDA)March 14, 2025
Viatris Specialty LLC1solutionNew drug applications (NDA)October 1, 2007

Dosage forms

Dosage formProductsShare
Solution6100%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)466.7%
New drug applications (NDA)116.7%
Authorized generics (NDA)116.7%

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.