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Data / Drug companies / Ethosuximide

Ethosuximide: 9 companies and 12 products in the FDA NDC directory

Ethosuximide is listed in the FDA National Drug Code Directory by 9 companies, with 12 products in commercial distribution. 11 of the products (91.7%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule; solution; capsule, liquid filled, and the newest product started marketing on November 12, 2021.

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.

Companies listing it
9
Products
12
Generic (ANDA) products
11 (91.7%)
Application numbers
8
Routes
Oral
Brand names
Zarontin
openFDA record search
api.fda.gov

Companies that list ethosuximide

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Chartwell RX, LLC2solution; capsuleGeneric drugs (ANDA)September 9, 2015
Epic Pharma, LLC2capsuleGeneric drugs (ANDA)November 12, 2021
Parke-Davis Div of Pfizer Inc2capsule; solutionNew drug applications (NDA)March 10, 2020
Bionpharma Inc.1capsule, liquid filledGeneric drugs (ANDA)October 21, 2016
Bryant Ranch Prepack1capsule, liquid filledGeneric drugs (ANDA)October 21, 2016
Chartwell Governmental & Specialty RX, LLC.1solutionGeneric drugs (ANDA)December 22, 2003
Mylan Pharmaceuticals Inc.1solutionGeneric drugs (ANDA)February 21, 2020
Pai Holdings, LLC DBA Pai Pharma1solutionGeneric drugs (ANDA)November 22, 2000
Strides Pharma Science Limited1capsuleGeneric drugs (ANDA)May 15, 2019

Dosage forms

Dosage formProductsShare
Capsule541.7%
Solution541.7%
Capsule, liquid filled216.7%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1191.7%
New drug applications (NDA)18.3%

Pharmacologic classes

ClassProducts
Anti-epileptic Agent12

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.