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Data / Drug companies / Suzetrigine

Suzetrigine: 2 companies and 2 products in the FDA NDC directory

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

Suzetrigine 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 tablet, film coated, and the newest product started marketing on January 30, 2025.

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

Companies that list suzetrigine

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Sportpharm LLC1tablet, film coatedNew drug applications (NDA)January 30, 2025
Vertex Pharmaceuticals Incorporated1tablet, film coatedNew drug applications (NDA)January 30, 2025

Dosage forms

Dosage formProductsShare
Tablet, film coated2100%

Marketing categories

Marketing categoryProductsShare
New drug applications (NDA)2100%

Pharmacologic classes

ClassProducts
Sodium Channel Blocker2

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.