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Data / Drug companies / United Therapeutics Corporation

United Therapeutics Corporation: 35 products in the FDA NDC directory, labeler code 66302

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

United Therapeutics Corporation (labeler code 66302) lists 35 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 35 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on November 7, 2025.

The request: Watch United Therapeutics Corporation (FDA labeler code 66302): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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.

Labeler code
66302
Products in commercial distribution
35
Packages
43
Finished drugs by generic name
4
Prescription products
35
Over the counter products
0
Flagged as original packager
35 of 35 products that carry the flag
Started marketing in the last 12 months
2
Earliest marketing start
May 22, 2002
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
New drug applications (NDA)3497.1%
Biologics (BLA)12.9%

Products by type

TypeProductsShare
Prescription drugs35100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Treprostinil326
Water140
Tadalafil154
Dinutuximab11

Dosage forms

Dosage formProductsShare
Kit1131.4%
Inhalant1131.4%
Injection, solution617.1%
Tablet, extended release514.3%
Tablet12.9%
Injection12.9%

Pharmacologic classes

FDA established pharmacologic classes of its products.

ClassProducts
Prostacycline Vasodilator21
Phosphodiesterase 5 Inhibitor1
Glycolipid Disialoganglioside-directed Antibody1

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Tyvaso DPI66302-670KitNew drug applications (NDA)November 7, 2025
Tyvaso DPI66302-660KitNew drug applications (NDA)November 7, 2025
Tyvaso DPI66302-780InhalantNew drug applications (NDA)October 24, 2024
Tyvaso DPI66302-680InhalantNew drug applications (NDA)October 24, 2024
Remodulin66302-114Injection, solutionNew drug applications (NDA)September 28, 2023
Tyvaso DPI66302-650KitNew drug applications (NDA)June 27, 2023
Tyvaso DPI66302-640KitNew drug applications (NDA)June 27, 2023
Tyvaso DPI66302-630KitNew drug applications (NDA)June 27, 2023
Orenitram66302-363KitNew drug applications (NDA)February 14, 2023
Orenitram66302-362KitNew drug applications (NDA)February 14, 2023
Orenitram66302-361KitNew drug applications (NDA)February 14, 2023
Tyvaso DPI66302-764InhalantNew drug applications (NDA)May 23, 2022
Tyvaso DPI66302-748InhalantNew drug applications (NDA)May 23, 2022
Tyvaso DPI66302-732InhalantNew drug applications (NDA)May 23, 2022
Tyvaso DPI66302-720KitNew drug applications (NDA)May 23, 2022
Tyvaso DPI66302-716InhalantNew drug applications (NDA)May 23, 2022
Tyvaso DPI66302-664InhalantNew drug applications (NDA)May 23, 2022
Tyvaso DPI66302-648InhalantNew drug applications (NDA)May 23, 2022
Tyvaso DPI66302-632InhalantNew drug applications (NDA)May 23, 2022
Tyvaso DPI66302-620KitNew drug applications (NDA)May 23, 2022
Tyvaso DPI66302-616InhalantNew drug applications (NDA)May 23, 2022
Tyvaso DPI66302-610KitNew drug applications (NDA)May 23, 2022
Unituxin66302-014InjectionBiologics (BLA)March 10, 2015
Sterile Diluent for Remodulin66302-150Injection, solutionNew drug applications (NDA)December 22, 2014
Orenitram66302-350Tablet, extended releaseNew drug applications (NDA)December 20, 2013

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.