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Data / Drug companies / Prostacycline Vasodilator

Prostacycline Vasodilator drugs: 2 drugs from 10 companies in the FDA NDC directory

Prostacycline Vasodilator is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 49 products in this class from 10 companies, covering 2 drugs by generic name. The main marketing category is new drug applications (NDA), 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.

  • 10Companies
  • 49Products
  • 2Drugs by generic name

Drugs in the Prostacycline Vasodilator class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Treprostinil416
Epoprostenol84

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
United Therapeutics Corporation21inhalant; injection, solutionNew drug applications (NDA)October 24, 2024
Alembic Pharmaceuticals Inc.4injection, solutionGeneric drugs (ANDA)February 11, 2021
Dr. Reddy's Laboratories Inc.4injection, solutionGeneric drugs (ANDA)February 13, 2023
Liquidia Technologies, Inc.4capsuleNew drug applications (NDA)May 23, 2025
Sandoz Inc4injectionGeneric drugs (ANDA)March 25, 2019
Teva Parenteral Medicines, Inc.4injection, solutionGeneric drugs (ANDA)September 30, 2019
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, solution1734.7%
Inhalant1122.4%
Injection, powder, lyophilized, for solution816.3%
Tablet, extended release510.2%
Capsule48.2%
Injection48.2%

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.