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Data / Drug companies / Hydroxychloroquine sulfate

Hydroxychloroquine sulfate: 33 companies and 57 products in the FDA NDC directory

Hydroxychloroquine sulfate is listed in the FDA National Drug Code Directory by 33 companies, with 57 products in commercial distribution. 52 of the products (91.2%) 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 May 8, 2025.

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Companies listing it
33
Products
57
Generic (ANDA) products
52 (91.2%)
Application numbers
12
Routes
Oral
Brand names
Plaquenil, Sovuna
openFDA record search
api.fda.gov

Companies that list hydroxychloroquine sulfate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Bryant Ranch Prepack8tablet, film coated; tabletGeneric drugs (ANDA)May 8, 2025
A-S Medication Solutions6tablet, film coated; tabletGeneric drugs (ANDA)May 12, 2020
Accord Healthcare Inc.4tabletGeneric drugs (ANDA)September 28, 2021
Aphena Pharma Solutions - Tennessee, LLC4tablet, film coated; tabletGeneric drugs (ANDA)May 17, 2018
Dr. Reddy's Laboratories Inc.4tablet, film coatedGeneric drugs (ANDA)October 24, 2022
Ani Pharmaceuticals, Inc.2tablet, film coatedNew drug applications (NDA)September 15, 2023
Cardinal Health 107, LLC2tablet, film coatedGeneric drugs (ANDA)May 1, 2018
NuCare Pharmaceuticals,Inc.2tablet, film coatedGeneric drugs (ANDA)October 1, 2019
Advanz Pharma (US) Corp.1tabletNew drug applications (NDA)June 28, 2013
American Health Packaging1tablet, film coatedGeneric drugs (ANDA)September 3, 2008
Amneal Pharmaceuticals NY LLC1tablet, film coatedGeneric drugs (ANDA)May 17, 2018
Amneal Pharmaceuticals NY LLC1tablet, film coatedGeneric drugs (ANDA)May 17, 2018
Aphena Pharma Solutions - Tennessee, LLC1tabletGeneric drugs (ANDA)May 8, 2025
Asclemed USA, Inc.1tablet, film coatedGeneric drugs (ANDA)October 1, 2019
Aurobindo Pharma Limited1tablet, film coatedGeneric drugs (ANDA)March 7, 2025
AvPAK1tablet, film coatedGeneric drugs (ANDA)May 15, 2020
Bryant Ranch Prepack1tabletGeneric drugs (ANDA)May 8, 2025
Bryant Ranch Prepack1tabletGeneric drugs (ANDA)October 24, 2022
Coupler LLC1tablet, film coatedGeneric drugs (ANDA)February 24, 2025
Creekwood Pharmaceuticals LLC1tabletGeneric drugs (ANDA)May 8, 2025
Ipca Laboratories Limited1tablet, film coatedGeneric drugs (ANDA)June 3, 2024
Laurus Labs Limited1tablet, film coatedGeneric drugs (ANDA)March 6, 2023
Major Pharmaceuticals1tablet, film coatedGeneric drugs (ANDA)May 1, 2018
NCS HealthCare of Ky, LLC DBA Vangard Labs1tablet, film coatedGeneric drugs (ANDA)January 3, 2008
NorthStar Rx LLC1tablet, film coatedGeneric drugs (ANDA)October 1, 2019
Preferred Pharmaceuticals Inc.1tablet, film coatedGeneric drugs (ANDA)July 1, 2020
Proficient Rx LP1tabletNew drug applications (NDA)June 28, 2013
Quallent Pharmaceuticals Health LLC1tablet, film coatedGeneric drugs (ANDA)September 30, 2022
Rising Pharma Holdings, Inc.1tablet, film coatedGeneric drugs (ANDA)May 29, 2023
Sun Pharmaceutical Industries, Inc.1tabletGeneric drugs (ANDA)June 18, 2018
Teva Pharmaceuticals USA, Inc.1tablet, film coatedGeneric drugs (ANDA)October 8, 2020
Zydus Lifesciences Limited1tablet, film coatedGeneric drugs (ANDA)January 3, 2008
Zydus Pharmaceuticals USA Inc.1tablet, film coatedGeneric drugs (ANDA)January 3, 2008

Dosage forms

Dosage formProductsShare
Tablet, film coated3968.4%
Tablet1831.6%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)5291.2%
New drug applications (NDA)58.8%

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.