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Data / Drug companies / Sumatriptan succinate

Sumatriptan succinate: 24 companies and 65 products in the FDA NDC directory

Sumatriptan succinate is listed in the FDA National Drug Code Directory by 24 companies, with 65 products in commercial distribution. 64 of the products (98.5%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; tablet, film coated; injection, and the newest product started marketing on November 6, 2025.

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Companies listing it
24
Products
65
Generic (ANDA) products
64 (98.5%)
Application numbers
12
Routes
Oral, Subcutaneous
Brand names
Sumatriptan, Zembrace SymTouch
openFDA record search
api.fda.gov

Companies that list sumatriptan succinate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
NuCare Pharmaceuticals,Inc.7tabletGeneric drugs (ANDA)June 18, 2018
Proficient Rx LP6tabletGeneric drugs (ANDA)November 17, 2009
A-S Medication Solutions4tablet; tablet, film coatedGeneric drugs (ANDA)August 17, 2009
Asclemed USA, Inc.4tabletGeneric drugs (ANDA)November 17, 2009
Dr. Reddy's Laboratories Limited4tablet; injectionGeneric drugs (ANDA)February 24, 2014
Sportpharm LLC4tablet; injectionGeneric drugs (ANDA)April 20, 2023
Aurobindo Pharma Limited3tabletGeneric drugs (ANDA)August 17, 2009
Direct_Rx3tablet, film coatedGeneric drugs (ANDA)December 2, 2024
Golden State Medical Supply, Inc.3tablet, film coatedGeneric drugs (ANDA)August 10, 2009
Mylan Pharmaceuticals Inc.3tablet, film coatedGeneric drugs (ANDA)August 10, 2009
NorthStar Rx LLC3tabletGeneric drugs (ANDA)June 18, 2018
Preferred Pharmaceuticals Inc.3tabletGeneric drugs (ANDA)October 24, 2016
Proficient Rx LP3tablet, film coated; injectionGeneric drugs (ANDA)August 10, 2009
Sun Pharmaceutical Industries, Inc.3tablet, film coatedGeneric drugs (ANDA)August 10, 2009
Alembic Pharmaceuticals Inc.2injectionGeneric drugs (ANDA)November 6, 2025
Alembic Pharmaceuticals Limited2injectionGeneric drugs (ANDA)November 6, 2025
Dr. Reddy's Laboratories Inc.1injectionGeneric drugs (ANDA)April 20, 2023
Fresenius Kabi USA, LLC1injectionGeneric drugs (ANDA)April 12, 2011
NorthStar RxLLC1injectionGeneric drugs (ANDA)June 13, 2023
Quality Care Products, LLC1tabletGeneric drugs (ANDA)February 4, 2021
Remedyrepack Inc.1tabletGeneric drugs (ANDA)May 14, 2018
Sun Pharmaceutical Industries, Inc.1injectionGeneric drugs (ANDA)August 20, 2025
Tonix Medicines, Inc.1solutionNew drug applications (NDA)July 1, 2023
Xellia Pharmaceuticals USA LLC1injectionGeneric drugs (ANDA)January 1, 2022

Dosage forms

Dosage formProductsShare
Tablet3756.9%
Tablet, film coated1523.1%
Injection1218.5%
Solution11.5%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)6498.5%
New drug applications (NDA)11.5%

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.