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Data / Drug companies / Amoxicillin

Amoxicillin: 35 companies and 278 products in the FDA NDC directory

Amoxicillin is listed in the FDA National Drug Code Directory by 35 companies, with 278 products in commercial distribution. 274 of the products (98.6%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule; powder, for suspension; tablet, film coated, and the newest product started marketing on September 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
35
Products
278
Generic (ANDA) products
274 (98.6%)
Application numbers
23
Routes
Oral
openFDA record search
api.fda.gov

Companies that list amoxicillin

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions45powder, for suspension; capsuleGeneric drugs (ANDA)September 15, 2014
NuCare Pharmaceuticals,Inc.38capsule; powder, for suspensionGeneric drugs (ANDA)April 1, 2024
Preferred Pharmaceuticals Inc.16powder, for suspension; tablet, film coatedGeneric drugs (ANDA)July 15, 2026
Chartwell RX, LLC15powder, for suspension; capsuleGeneric drugs (ANDA)June 18, 2007
Remedyrepack Inc.15capsule; tablet, film coatedGeneric drugs (ANDA)December 2, 2025
Asclemed USA, Inc.12capsule; powder, for suspensionGeneric drugs (ANDA)December 12, 2017
Bryant Ranch Prepack12capsule; tablet, film coatedGeneric drugs (ANDA)November 9, 2005
Proficient Rx LP11powder, for suspension; tablet, film coatedGeneric drugs (ANDA)March 26, 2007
Teva Pharmaceuticals USA, Inc.9powder, for suspension; tablet, film coatedGeneric drugs (ANDA)April 2, 2003
Aurobindo Pharma Limited8powder, for suspension; tablet, film coatedGeneric drugs (ANDA)September 15, 2014
Proficient Rx LP8powder, for suspension; capsuleGeneric drugs (ANDA)March 26, 2007
Sandoz Inc8powder, for suspension; tablet, film coatedGeneric drugs (ANDA)March 26, 2007
Redpharm Drug7capsule; tablet, coatedGeneric drugs (ANDA)September 15, 2022
Hikma Pharmaceuticals USA Inc.6powder, for suspension; tablet, coatedGeneric drugs (ANDA)March 1, 2007
Rising Pharma Holdings, Inc.6tablet, film coated; capsuleGeneric drugs (ANDA)December 28, 2006
Coupler LLC5capsule; tablet, film coatedGeneric drugs (ANDA)August 3, 2026
Hawaii Repack, Inc.5powder, for suspension; capsuleGeneric drugs (ANDA)March 26, 2007
PD-Rx Pharmaceuticals, Inc.5capsule; tablet, coatedGeneric drugs (ANDA)March 29, 2006
QPharma, Inc.5capsule; tablet, film coatedGeneric drugs (ANDA)November 9, 2005
Sportpharm LLC5capsuleGeneric drugs (ANDA)August 16, 2023
American Health Packaging4tablet, film coated; capsuleGeneric drugs (ANDA)March 25, 2025
Northwind Health Company, LLC4capsule; tablet, chewableGeneric drugs (ANDA)September 15, 2026
NuCare Pharmaceuticals, Inc.4tablet, chewable; powder, for suspensionGeneric drugs (ANDA)June 19, 2006
PD-Rx Pharmaceuticals, Inc.4capsule; tablet, coatedGeneric drugs (ANDA)March 1, 2007
USAntibiotics, LLC4capsule; for suspensionGeneric drugs (ANDA)May 15, 2025
Chartwell Governmental & Specialty RX, LLC.3capsuleGeneric drugs (ANDA)September 30, 1990
Proficient Rx LP3capsule; powder, for suspensionGeneric drugs (ANDA)November 1, 2022
Direct_Rx2tablet, film coated; powder, for suspensionGeneric drugs (ANDA)April 17, 2023
Micro Labs Limited2capsuleGeneric drugs (ANDA)November 1, 2022
NorthStar Rx LLC2capsuleGeneric drugs (ANDA)November 9, 2005
Advanced Rx of Tennessee, LLC1capsuleGeneric drugs (ANDA)February 15, 2023
Asclemed USA Inc.1for suspensionAuthorized generics (NDA)April 1, 2024
Direct RX1powder, for suspensionGeneric drugs (ANDA)January 1, 2014
Health Department, Oklahoma State1capsuleGeneric drugs (ANDA)November 9, 2005
PD-Rx Pharmaceuticals, Inc.1tablet, chewableGeneric drugs (ANDA)January 1, 1993

Dosage forms

Dosage formProductsShare
Capsule12344.2%
Powder, for suspension8932%
Tablet, film coated4014.4%
Tablet, chewable124.3%
Tablet, coated103.6%
For suspension41.4%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)27498.6%
Authorized generics (NDA)41.4%

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.