Skip to the page

Data / Drug companies / Sucralfate

Sucralfate: 39 companies and 63 products in the FDA NDC directory

Sucralfate is listed in the FDA National Drug Code Directory by 39 companies, with 63 products in commercial distribution. 52 of the products (82.5%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; suspension, and the newest product started marketing on July 16, 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
39
Products
63
Generic (ANDA) products
52 (82.5%)
Application numbers
12
Routes
Oral
Brand names
Carafate
openFDA record search
api.fda.gov

Companies that list sucralfate

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Advanced Rx of Tennessee, LLC4tabletGeneric drugs (ANDA)March 13, 2023
A-S Medication Solutions3tabletGeneric drugs (ANDA)May 20, 2023
Bryant Ranch Prepack3tabletGeneric drugs (ANDA)February 17, 2020
Bryant Ranch Prepack3tabletGeneric drugs (ANDA)May 20, 2023
Cardinal Health 107, LLC3tablet; suspensionGeneric drugs (ANDA)July 10, 2026
NuCare Pharmaceuticals,Inc.3tabletGeneric drugs (ANDA)May 20, 2023
Preferred Pharmaceuticals Inc.3tabletGeneric drugs (ANDA)December 10, 2024
Allergan, Inc.2tablet; suspensionNew drug applications (NDA)December 16, 1993
Aphena Pharma Solutions - Tennessee, LLC2tabletGeneric drugs (ANDA)February 17, 2020
Bryant Ranch Prepack2tablet; suspensionGeneric drugs (ANDA)July 10, 2024
Chartwell RX, LLC2suspension; tabletGeneric drugs (ANDA)April 14, 2025
Direct_Rx2tabletGeneric drugs (ANDA)March 2, 2023
NCS HealthCare of Ky, LLC DBA Vangard Labs2tabletGeneric drugs (ANDA)May 20, 2023
Northwind Health Company, LLC2tabletGeneric drugs (ANDA)November 18, 2020
Proficient Rx LP2tabletGeneric drugs (ANDA)February 17, 2020
Safecor Health, LLC2tablet; suspensionGeneric drugs (ANDA)July 16, 2026
American Health Packaging1suspensionGeneric drugs (ANDA)August 1, 2023
Amneal Pharmaceuticals NY LLC1tabletGeneric drugs (ANDA)April 22, 2022
Amneal Pharmaceuticals NY LLC1tabletGeneric drugs (ANDA)March 2, 2024
Asclemed USA Inc.1tabletGeneric drugs (ANDA)November 11, 1996
Atlantic Biologicals Corp.1suspensionGeneric drugs (ANDA)March 15, 2022
AvKARE1tabletGeneric drugs (ANDA)October 31, 2023
Chartwell Governmental & Specialty RX, LLC.1suspensionGeneric drugs (ANDA)April 14, 2025
Cosette Pharmaceuticals, Inc.1suspensionGeneric drugs (ANDA)December 19, 2024
Coupler LLC1tabletGeneric drugs (ANDA)February 4, 2025
Glenmark Pharmaceuticals Inc., USA1suspensionGeneric drugs (ANDA)January 5, 2026
Kesin Pharma Corporation1suspensionGeneric drugs (ANDA)July 1, 2024
Mylan Institutional Inc.1tabletGeneric drugs (ANDA)September 24, 2013
Mylan Pharmaceuticals Inc.1tabletAuthorized generics (NDA)September 25, 2017
Pacific Pharma, Inc.1suspensionAuthorized generics (NDA)February 1, 2024
Pai Holdings, LLC DBA Pai Pharma1suspensionGeneric drugs (ANDA)March 15, 2022
Redpharm Drug1tabletGeneric drugs (ANDA)May 20, 2023
Richmond Pharmaceuticals, Inc.1suspensionGeneric drugs (ANDA)November 21, 2024
Strides Pharma Science Limited1suspensionGeneric drugs (ANDA)July 10, 2024
Teva Pharmaceuticals USA, Inc.1tabletGeneric drugs (ANDA)November 11, 1996
Torrent Pharmaceuticals Limited1suspensionGeneric drugs (ANDA)September 15, 2025
Viona Pharmaceuticals Inc1tabletGeneric drugs (ANDA)May 20, 2023
VistaPharm, LLC1suspensionGeneric drugs (ANDA)March 15, 2022
Zydus Lifesciences Limited1tabletGeneric drugs (ANDA)May 20, 2023

Dosage forms

Dosage formProductsShare
Tablet4673%
Suspension1727%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)5282.5%
Authorized generics (NDA)914.3%
New drug applications (NDA)23.2%

Pharmacologic classes

ClassProducts
Aluminum Complex63

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.