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Data / Drug companies / Eltrombopag

Eltrombopag: 11 companies and 45 products in the FDA NDC directory

Eltrombopag is listed in the FDA National Drug Code Directory by 11 companies, with 45 products in commercial distribution. 41 of the products (91.1%) 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 October 15, 2026.

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Companies listing it
11
Products
45
Generic (ANDA) products
41 (91.1%)
Application numbers
8
Routes
Oral
Brand names
Alvaiz
openFDA record search
api.fda.gov

Companies that list eltrombopag

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Teva Pharmaceuticals, Inc.8tablet, film coatedGeneric drugs (ANDA)September 17, 2026
Amneal Pharmaceuticals NY LLC4tablet, film coatedGeneric drugs (ANDA)January 15, 2026
Amneal Pharmaceuticals NY LLC4tablet, film coatedGeneric drugs (ANDA)January 15, 2026
AvKARE4tablet, film coatedGeneric drugs (ANDA)February 16, 2026
Camber Pharmaceuticals, Inc.4tablet, film coatedGeneric drugs (ANDA)May 13, 2025
Dr. Reddy's Laboratories Inc.4tablet, film coatedGeneric drugs (ANDA)March 17, 2026
Quallent Pharmaceuticals Health LLC4tablet, film coatedGeneric drugs (ANDA)October 15, 2026
XLCare Pharmaceuticals, Inc.4tablet, film coatedGeneric drugs (ANDA)August 7, 2025
Zydus Lifesciences Limited4tabletGeneric drugs (ANDA)January 14, 2026
Zydus Pharmaceuticals USA Inc.4tabletGeneric drugs (ANDA)January 14, 2026
Biocon Pharma Inc.1tablet, film coatedGeneric drugs (ANDA)September 9, 2026

Dosage forms

Dosage formProductsShare
Tablet, film coated3782.2%
Tablet817.8%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)4191.1%
New drug applications (NDA)48.9%

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.