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Data / Drug companies / Eletriptan hydrobromide

Eletriptan hydrobromide: 11 companies and 19 products in the FDA NDC directory

Eletriptan hydrobromide is listed in the FDA National Drug Code Directory by 11 companies, with 19 products in commercial distribution. 17 of the products (89.5%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet, and the newest product started marketing on May 13, 2026.

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Companies listing it
11
Products
19
Generic (ANDA) products
17 (89.5%)
Application numbers
7
Routes
Oral
Brand names
Relpax
openFDA record search
api.fda.gov

Companies that list eletriptan hydrobromide

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Apnar Pharma LP2tablet, film coatedGeneric drugs (ANDA)May 13, 2026
Aurobindo Pharma Limited2tablet, film coatedGeneric drugs (ANDA)January 15, 2019
Camber Pharmaceuticals, Inc.2tablet, film coatedGeneric drugs (ANDA)July 7, 2025
Mylan Pharmaceuticals Inc.2tablet, film coatedGeneric drugs (ANDA)August 15, 2017
Teva Pharmaceuticals USA, Inc.2tablet, film coatedGeneric drugs (ANDA)July 21, 2017
Viatris Specialty LLC2tabletNew drug applications (NDA)May 8, 2025
Zydus Lifesciences Limited2tablet, film coatedGeneric drugs (ANDA)July 12, 2017
Zydus Pharmaceuticals USA Inc.2tablet, film coatedGeneric drugs (ANDA)July 12, 2017
Advanced Rx of Tennessee, LLC1tablet, film coatedGeneric drugs (ANDA)June 25, 2024
Bryant Ranch Prepack1tablet, film coatedGeneric drugs (ANDA)February 16, 2018
Bryant Ranch Prepack1tablet, film coatedGeneric drugs (ANDA)July 12, 2017

Dosage forms

Dosage formProductsShare
Tablet, film coated1789.5%
Tablet210.5%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1789.5%
New drug applications (NDA)210.5%

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.