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Data / Drug companies / Capecitabine

Capecitabine: 19 companies and 34 products in the FDA NDC directory

Capecitabine is listed in the FDA National Drug Code Directory by 19 companies, with 34 products in commercial distribution. 33 of the products (97.1%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet, and the newest product started marketing on June 26, 2025.

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
19
Products
34
Generic (ANDA) products
33 (97.1%)
Application numbers
12
Routes
Oral
Brand names
Xeloda
openFDA record search
api.fda.gov

Companies that list capecitabine

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Accord Healthcare Inc.2tablet, film coatedGeneric drugs (ANDA)June 9, 2015
Armas Pharmaceuticals Inc.2tablet, film coatedGeneric drugs (ANDA)March 1, 2019
Ascend Laboratories, LLC2tablet, film coatedGeneric drugs (ANDA)November 25, 2017
Aurobindo Pharma Limited2tabletGeneric drugs (ANDA)April 17, 2018
BluePoint Laboratories2tablet, film coatedGeneric drugs (ANDA)April 22, 2025
Camber Pharmaceuticals, Inc.2tablet, film coatedGeneric drugs (ANDA)March 5, 2024
Cipla USA Inc.2tablet, film coatedGeneric drugs (ANDA)July 1, 2023
CivicaScript LLC2tablet, film coatedGeneric drugs (ANDA)June 26, 2025
Dr. Reddy's Laboratories Limited2tabletGeneric drugs (ANDA)December 10, 2020
Golden State Medical Supply, Inc.2tablet, film coatedGeneric drugs (ANDA)September 16, 2013
Lifestar Pharma LLC2tablet, film coatedGeneric drugs (ANDA)September 1, 2020
Novadoz Pharmaceuticals LLC2tablet, film coatedGeneric drugs (ANDA)July 21, 2018
Sun Pharmaceutical Industries, Inc.2tablet, film coatedGeneric drugs (ANDA)September 1, 2019
Teva Pharmaceuticals USA, Inc.2tablet, film coatedGeneric drugs (ANDA)March 7, 2014
Teyro Labs Private Limited2tablet, film coatedGeneric drugs (ANDA)February 16, 2022
American Health Packaging1tablet, film coatedGeneric drugs (ANDA)March 7, 2016
H2-Pharma, LLC1tablet, film coatedNew drug applications (NDA)April 30, 1998
NorthStar RxLLC1tablet, film coatedGeneric drugs (ANDA)December 1, 2024
Quallent Pharmaceuticals Health LLC1tabletGeneric drugs (ANDA)July 21, 2023

Dosage forms

Dosage formProductsShare
Tablet, film coated2985.3%
Tablet514.7%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)3397.1%
New drug applications (NDA)12.9%

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.