Skip to the page

Data / Drug companies / Etodolac

Etodolac: 31 companies and 104 products in the FDA NDC directory

Etodolac is listed in the FDA National Drug Code Directory by 31 companies, with 104 products in commercial distribution. 104 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; capsule; tablet, film coated, extended release, and the newest product started marketing on July 15, 2026.

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
31
Products
104
Generic (ANDA) products
104 (100.0%)
Application numbers
14
Routes
Oral
openFDA record search
api.fda.gov

Companies that list etodolac

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions9tablet, film coated; capsuleGeneric drugs (ANDA)February 13, 2026
Bryant Ranch Prepack7tablet, film coated; capsuleGeneric drugs (ANDA)August 1, 2021
Sun Pharmaceutical Industries, Inc.7tablet, extended release; tablet, film coatedGeneric drugs (ANDA)March 13, 2003
Advanced Rx of Tennessee, LLC6tablet, film coated; tablet, extended releaseGeneric drugs (ANDA)August 29, 2025
Aphena Pharma Solutions - Tennessee, LLC6tablet, film coatedGeneric drugs (ANDA)June 11, 2018
Golden State Medical Supply, Inc.6tablet, extended release; tablet, film coatedGeneric drugs (ANDA)March 13, 2003
Bryant Ranch Prepack5capsule; tablet, film coated, extended releaseGeneric drugs (ANDA)March 9, 2015
Apotex Corp.4tablet, film coated; capsuleGeneric drugs (ANDA)May 1, 2003
Ipca Laboratories Limited4capsule; tabletGeneric drugs (ANDA)February 13, 2026
NorthStar Rx LLC3tablet, extended releaseGeneric drugs (ANDA)March 13, 2003
Northwind Health Company, LLC3tablet, film coated; capsuleGeneric drugs (ANDA)July 8, 2021
PD-Rx Pharmaceuticals, Inc.3tablet, film coatedGeneric drugs (ANDA)May 1, 2003
Preferred Pharmaceuticals Inc.3tablet, film coatedGeneric drugs (ANDA)March 24, 2025
Proficient Rx LP3tablet, film coated; tablet, film coated, extended releaseGeneric drugs (ANDA)March 9, 2015
Proficient Rx LP3tablet, film coated, extended release; tablet, extended releaseGeneric drugs (ANDA)February 15, 2014
Remedyrepack Inc.3tablet, film coatedGeneric drugs (ANDA)December 30, 2025
Teva Pharmaceuticals USA, Inc.3tablet, film coated, extended releaseGeneric drugs (ANDA)February 9, 2001
Zydus Lifesciences Limited3tablet, film coated, extended releaseGeneric drugs (ANDA)February 15, 2014
Zydus Pharmaceuticals USA Inc.3tablet, film coated, extended releaseGeneric drugs (ANDA)February 15, 2014
Amneal Pharmaceuticals NY LLC2tablet, film coatedGeneric drugs (ANDA)June 11, 2018
Ani Pharmaceuticals, Inc.2capsuleGeneric drugs (ANDA)March 9, 2015
Aurobindo Pharma Limited2tablet, film coatedGeneric drugs (ANDA)July 15, 2026
Bryant Ranch Prepack2capsuleGeneric drugs (ANDA)March 9, 2015
Chartwell RX, LLC2tablet, film coatedGeneric drugs (ANDA)December 7, 2018
Edenbridge Pharmaceuticals LLC.2tablet, film coatedGeneric drugs (ANDA)December 7, 2018
St. Mary's Medical Park Pharmacy2tablet, film coated, extended release; tablet, film coatedGeneric drugs (ANDA)March 14, 2018
Unichem Pharmaceuticals (USA), Inc.2tablet, film coatedGeneric drugs (ANDA)August 1, 2021
Doc Rx1tablet, film coatedGeneric drugs (ANDA)June 11, 2018
Medsource Pharmaceuticals1tablet, film coatedGeneric drugs (ANDA)May 1, 2003
NuCare Pharmaceuticals,Inc.1tablet, film coated, extended releaseGeneric drugs (ANDA)February 15, 2014
PD-Rx Pharmaceuticals, Inc.1tablet, film coatedGeneric drugs (ANDA)May 1, 2003

Dosage forms

Dosage formProductsShare
Tablet, film coated5552.9%
Capsule2019.2%
Tablet, film coated, extended release1514.4%
Tablet, extended release1110.6%
Tablet32.9%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)104100%

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.