Skip to the page

Data / Drug companies / Epoprostenol

Epoprostenol: 4 companies and 8 products in the FDA NDC directory

Epoprostenol is listed in the FDA National Drug Code Directory by 4 companies, with 8 products in commercial distribution. 6 of the products (75.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection, powder, lyophilized, for solution, and the newest product started marketing on December 29, 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
4
Products
8
Generic (ANDA) products
6 (75.0%)
Application numbers
4
Routes
Intravenous
Brand names
Veletri
openFDA record search
api.fda.gov

Companies that list epoprostenol

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Actelion Pharmaceuticals US, Inc.2injection, powder, lyophilized, for solutionNew drug applications (NDA)April 22, 2010
Gland Pharma Limited2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)December 29, 2025
Mylan Institutional LLC2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)September 25, 2024
Sun Pharmaceutical Industries, Inc.2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)January 16, 2021

Dosage forms

Dosage formProductsShare
Injection, powder, lyophilized, for solution8100%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)675%
New drug applications (NDA)225%

Pharmacologic classes

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.