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Data / Drug companies / Etoposide

Etoposide: 9 companies and 18 products in the FDA NDC directory

Etoposide is listed in the FDA National Drug Code Directory by 9 companies, with 18 products in commercial distribution. 14 of the products (77.8%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection; injection, solution, concentrate; capsule, and the newest product started marketing on September 14, 2026.

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Companies listing it
9
Products
18
Generic (ANDA) products
14 (77.8%)
Application numbers
7
Routes
Intravenous, Oral
Brand names
VePesid, Avopef
openFDA record search
api.fda.gov

Companies that list etoposide

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
BluePoint Laboratories4injection, solution, concentrate; injectionGeneric drugs (ANDA)December 1, 2025
Hikma Pharmaceuticals USA Inc.4injectionGeneric drugs (ANDA)February 1, 1997
Meitheal Pharmaceuticals Inc.3injection, solution, concentrateGeneric drugs (ANDA)February 1, 2025
Avyxa Pharma, LLC2injectionNew drug applications (NDA)September 14, 2026
Accord Healthcare Inc.1injectionGeneric drugs (ANDA)March 3, 2015
Amneal Pharmaceuticals NY LLC1capsuleAuthorized generics (NDA)May 15, 2026
Fresenius Kabi USA, LLC1injection, solutionGeneric drugs (ANDA)July 18, 2001
Mylan Pharmaceuticals Inc.1capsuleGeneric drugs (ANDA)October 22, 2001
Onesource Specialty Pharma Limited1capsuleNew drug applications (NDA)May 29, 2026

Dosage forms

Dosage formProductsShare
Injection844.4%
Injection, solution, concentrate633.3%
Capsule316.7%
Injection, solution15.6%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1477.8%
New drug applications (NDA)316.7%
Authorized generics (NDA)15.6%

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.