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Data / Drug companies / Valsartan

Valsartan: 38 companies and 143 products in the FDA NDC directory

Valsartan is listed in the FDA National Drug Code Directory by 38 companies, with 143 products in commercial distribution. 136 of the products (95.1%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet; solution, and the newest product started marketing on August 24, 2026.

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Companies listing it
38
Products
143
Generic (ANDA) products
136 (95.1%)
Application numbers
19
Routes
Oral
Brand names
Diovan
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api.fda.gov

Companies that list valsartan

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Bryant Ranch Prepack11tablet, film coated; tabletGeneric drugs (ANDA)June 23, 2021
A-S Medication Solutions9tablet; tablet, film coatedGeneric drugs (ANDA)June 23, 2021
Camber Pharmaceuticals, Inc.8tablet, film coatedGeneric drugs (ANDA)June 23, 2021
Novartis Pharmaceuticals Corporation7tabletNew drug applications (NDA)July 1, 2001
Northwind Health Company, LLC5tablet, film coated; tabletGeneric drugs (ANDA)August 15, 2023
Alembic Pharmaceuticals Inc.4tabletGeneric drugs (ANDA)May 20, 2016
Alembic Pharmaceuticals Limited4tabletGeneric drugs (ANDA)January 6, 2015
Amneal Pharmaceuticals LLC4tabletGeneric drugs (ANDA)January 27, 2016
Amneal Pharmaceuticals of New York LLC4tabletGeneric drugs (ANDA)August 1, 2023
Ascend Laboratories, LLC4tablet, film coatedGeneric drugs (ANDA)March 14, 2019
Aurobindo Pharma Limited4tablet, film coatedGeneric drugs (ANDA)January 5, 2015
AvKARE4tabletGeneric drugs (ANDA)June 23, 2020
AvPAK4tablet, film coatedGeneric drugs (ANDA)October 24, 2023
Dr. Reddy's Laboratories Limited4tablet, film coatedGeneric drugs (ANDA)March 30, 2018
Jubilant Cadista Pharmaceuticals Inc.4tabletGeneric drugs (ANDA)August 24, 2026
Kesin Pharma Corporation4tablet, film coatedGeneric drugs (ANDA)March 14, 2019
Laurus Labs Limited4tablet, film coatedGeneric drugs (ANDA)April 22, 2026
Macleods Pharmaceuticals Limited4tablet, film coatedGeneric drugs (ANDA)September 19, 2016
Mylan Pharmaceuticals Inc.4tablet, film coatedGeneric drugs (ANDA)January 5, 2015
Ohm Laboratories Inc.4tablet, film coatedGeneric drugs (ANDA)July 7, 2014
ScieGen Pharmaceuticals, Inc.4tabletGeneric drugs (ANDA)October 27, 2021
Solco Healthcare US, LLC4tabletGeneric drugs (ANDA)August 31, 2015
Square Pharmaceuticals Limited4tabletGeneric drugs (ANDA)July 15, 2022
Unichem Pharmaceuticals (USA), Inc.4tablet, film coatedGeneric drugs (ANDA)May 4, 2018
Viona Pharmaceuticals Inc4tablet, film coatedGeneric drugs (ANDA)August 30, 2024
Zydus Lifesciences Limited4tablet, film coatedGeneric drugs (ANDA)August 30, 2024
American Health Packaging3tablet, film coatedGeneric drugs (ANDA)June 29, 2021
Aphena Pharma Solutions - Tennessee, LLC2tabletGeneric drugs (ANDA)June 23, 2020
Coupler LLC2tablet, film coatedGeneric drugs (ANDA)September 16, 2025
Direct_Rx2tablet, film coatedGeneric drugs (ANDA)April 26, 2024
Northwind Health Company, LLC2tablet, film coatedGeneric drugs (ANDA)September 5, 2023
PD-Rx Pharmaceuticals, Inc.2tablet, film coated; tabletGeneric drugs (ANDA)August 30, 2024
Ani Pharmaceuticals, Inc.1solutionGeneric drugs (ANDA)November 2, 2021
Lifsa Drugs LLC1solutionGeneric drugs (ANDA)April 4, 2022
Lupin Pharmaceuticals, Inc.1tabletGeneric drugs (ANDA)January 5, 2015
Proficient Rx LP1tablet, film coatedGeneric drugs (ANDA)June 23, 2021
Proficient Rx LP1tablet, film coatedGeneric drugs (ANDA)September 19, 2016
Proficient Rx LP1tabletGeneric drugs (ANDA)August 31, 2015

Dosage forms

Dosage formProductsShare
Tablet, film coated8257.3%
Tablet5941.3%
Solution21.4%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)13695.1%
New drug applications (NDA)74.9%

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.