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Data / Drug companies / Fluorometholone acetate

Fluorometholone acetate: 2 companies and 2 products in the FDA NDC directory

Fluorometholone acetate is listed in the FDA National Drug Code Directory by 2 companies, with 2 products in commercial distribution. 0 of the products (0.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are suspension/ drops, and the newest product started marketing on March 31, 2025.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Companies listing it
2
Products
2
Generic (ANDA) products
0 (0.0%)
Application numbers
1
Routes
Ophthalmic
Brand names
Flarex
openFDA record search
api.fda.gov

Companies that list fluorometholone acetate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Eyevance Pharmaceuticals1suspension/ dropsNew drug applications (NDA)March 5, 2019
Harrow Eye, LLC1suspension/ dropsNew drug applications (NDA)March 31, 2025

Dosage forms

Dosage formProductsShare
Suspension/ drops2100%

Marketing categories

Marketing categoryProductsShare
New drug applications (NDA)2100%

Pharmacologic classes

ClassProducts
Corticosteroid2

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