Skip to the page

Data / Drug companies / Cephalexin

Cephalexin: 36 companies and 184 products in the FDA NDC directory

Cephalexin is listed in the FDA National Drug Code Directory by 36 companies, with 184 products in commercial distribution. 184 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule; for suspension; powder, for suspension, and the newest product started marketing on August 12, 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
36
Products
184
Generic (ANDA) products
184 (100.0%)
Application numbers
14
Routes
Oral
openFDA record search
api.fda.gov

Companies that list cephalexin

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Bryant Ranch Prepack28capsule; for suspensionGeneric drugs (ANDA)March 28, 2019
A-S Medication Solutions17capsule; for suspensionGeneric drugs (ANDA)March 28, 2019
NuCare Pharmaceuticals,Inc.16capsule; for suspensionGeneric drugs (ANDA)March 28, 2019
Asclemed USA, Inc.11capsuleGeneric drugs (ANDA)September 7, 2023
Remedyrepack Inc.9capsule; for suspensionGeneric drugs (ANDA)October 28, 2025
Ascend Laboratories, LLC8capsule; tabletGeneric drugs (ANDA)October 21, 2024
Bryant Ranch Prepack7capsule; for suspensionGeneric drugs (ANDA)March 28, 2019
Bryant Ranch Prepack7capsule; for suspensionGeneric drugs (ANDA)March 28, 2019
Preferred Pharmaceuticals Inc.7capsule; for suspensionGeneric drugs (ANDA)August 12, 2026
Teva Pharmaceuticals USA, Inc.6tablet; powder, for suspensionGeneric drugs (ANDA)September 30, 1990
Aurobindo Pharma Limited5powder, for suspension; tablet, film coatedGeneric drugs (ANDA)June 9, 2026
Advanced Rx of Tennessee, LLC4capsuleGeneric drugs (ANDA)September 14, 2022
AvKARE4capsuleGeneric drugs (ANDA)April 24, 2026
Chartwell RX, LLC4capsule; powder, for suspensionGeneric drugs (ANDA)February 28, 2018
Hawaii Repack, Inc.4capsuleGeneric drugs (ANDA)June 4, 2012
Lupin Pharmaceuticals, Inc.4capsule; for suspensionGeneric drugs (ANDA)September 6, 2017
PD-Rx Pharmaceuticals, Inc.4capsuleGeneric drugs (ANDA)January 20, 2011
QPharma, Inc.4capsuleGeneric drugs (ANDA)January 20, 2011
Direct RX3capsuleGeneric drugs (ANDA)August 14, 2019
Proficient Rx LP3capsule; for suspensionGeneric drugs (ANDA)September 6, 2017
Sportpharm LLC3capsuleGeneric drugs (ANDA)July 21, 2021
American Health Packaging2capsuleGeneric drugs (ANDA)October 19, 2015
Aurobindo Pharma Limited2capsuleGeneric drugs (ANDA)November 16, 2005
AvPAK2capsuleGeneric drugs (ANDA)September 15, 2014
Coupler LLC2capsuleGeneric drugs (ANDA)April 28, 2026
Cronus Pharma LLC2capsuleGeneric drugs (ANDA)November 16, 2005
Major Pharmaceuticals2capsuleGeneric drugs (ANDA)November 6, 2023
Northwind Health Company, LLC2capsuleGeneric drugs (ANDA)November 26, 2025
PD-Rx Pharmaceuticals, Inc.2capsuleGeneric drugs (ANDA)September 30, 1990
PD-Rx Pharmaceuticals, Inc.2capsuleGeneric drugs (ANDA)January 20, 2011
Pharma-C, Inc.2capsuleGeneric drugs (ANDA)October 15, 2010
Proficient Rx LP2capsule; powder, for suspensionGeneric drugs (ANDA)January 11, 2006
Amella Pharma, LLC1capsuleGeneric drugs (ANDA)June 27, 2018
NuCare Pharmaceuticals, Inc.1powder, for suspensionGeneric drugs (ANDA)September 30, 1990
Proficient Rx LP1capsuleGeneric drugs (ANDA)November 16, 2005
Unit Dose Solutions, Inc.1capsuleGeneric drugs (ANDA)September 30, 1990

Dosage forms

Dosage formProductsShare
Capsule14277.2%
For suspension2815.2%
Powder, for suspension84.3%
Tablet42.2%
Tablet, film coated21.1%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)184100%

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.