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Data / Drug companies / Erythromycin

Erythromycin: 36 companies and 81 products in the FDA NDC directory

Erythromycin is listed in the FDA National Drug Code Directory by 36 companies, with 81 products in commercial distribution. 79 of the products (97.5%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; ointment; tablet, delayed release, and the newest product started marketing on April 1, 2026.

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Companies listing it
36
Products
81
Generic (ANDA) products
79 (97.5%)
Application numbers
19
Routes
Oral, Ophthalmic, Topical
Brand names
Ery-Tab, Ery
openFDA record search
api.fda.gov

Companies that list erythromycin

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Azurity Pharmaceuticals, Inc.6tablet, delayed release; tablet, film coatedGeneric drugs (ANDA)January 10, 2012
Amneal Pharmaceuticals NY LLC5tablet, delayed release; suspensionGeneric drugs (ANDA)November 4, 2019
Torrent Pharmaceuticals Limited5tablet, delayed release; tablet, coatedGeneric drugs (ANDA)October 21, 2024
Wilshire Pharmaceuticals, Inc.5tablet, delayed release; tablet, film coatedGeneric drugs (ANDA)July 22, 2019
Golden State Medical Supply, Inc.4tablet, coated; tablet, delayed releaseGeneric drugs (ANDA)July 26, 2021
NuCare Pharmaceuticals,Inc.4ointment; solutionGeneric drugs (ANDA)October 18, 2023
A-S Medication Solutions3ointment; tablet, film coatedGeneric drugs (ANDA)May 4, 2021
Asclemed USA, Inc.3ointmentGeneric drugs (ANDA)May 8, 2014
Bryant Ranch Prepack3solution; swabGeneric drugs (ANDA)December 19, 2011
Bryant Ranch Prepack3gel; swabGeneric drugs (ANDA)July 7, 2008
Padagis Israel Pharmaceuticals Ltd3gel; swabGeneric drugs (ANDA)December 19, 2011
Alembic Pharmaceuticals Inc.2tablet, film coatedGeneric drugs (ANDA)August 28, 2023
Alembic Pharmaceuticals Limited2tablet, film coatedGeneric drugs (ANDA)August 28, 2023
Amneal Pharmaceuticals NY LLC2suspensionGeneric drugs (ANDA)December 2, 2023
Ascend Laboratories, LLC2tablet, film coatedGeneric drugs (ANDA)July 14, 2022
Cadila Pharmaceuticals Limited2tablet, film coatedGeneric drugs (ANDA)October 6, 2021
Modavar Pharmaceuticals LLC2tablet, film coatedGeneric drugs (ANDA)July 31, 2021
Orange Pharmaceuticals USA LLC2tablet, film coatedGeneric drugs (ANDA)October 5, 2019
Proficient Rx LP2ointmentGeneric drugs (ANDA)July 18, 1996
Redpharm Drug2ointmentGeneric drugs (ANDA)April 1, 2026
Teva Pharmaceuticals USA, Inc.2tablet, film coatedGeneric drugs (ANDA)May 4, 2021
Zydus Lifesciences Limited2tablet, film coatedGeneric drugs (ANDA)June 30, 2023
Zydus Pharmaceuticals USA Inc.2tablet, film coatedGeneric drugs (ANDA)June 30, 2023
Armas Pharmaceuticals Inc.1ointmentGeneric drugs (ANDA)October 18, 2023
Bausch & Lomb Incorporated1ointmentGeneric drugs (ANDA)July 29, 1994
Cardinal Health 107, LLC1ointmentGeneric drugs (ANDA)July 29, 1994
Direct RX1ointmentGeneric drugs (ANDA)January 1, 2014
Dr. Reddy's Laboratories Inc.1capsule, delayed release pelletsAuthorized generics (NDA)September 1, 2024
Fera Pharmaceuticals, LLC1ointmentUnapproved drugs for a shortageSeptember 27, 2023
NuCare Pharmaceuticals, Inc.1ointmentGeneric drugs (ANDA)July 29, 1994
PD-Rx Pharmaceuticals, Inc.1tablet, film coatedGeneric drugs (ANDA)September 6, 2011
Preferred Pharmaceuticals Inc.1ointmentGeneric drugs (ANDA)April 2, 2015
Remedyrepack Inc.1ointmentGeneric drugs (ANDA)April 26, 2017
Sentiss Pharmaceuticals LLC1ointmentGeneric drugs (ANDA)April 1, 2026
Sportpharm LLC1ointmentGeneric drugs (ANDA)July 29, 1994
St. Mary's Medical Park Pharmacy1ointmentGeneric drugs (ANDA)October 18, 2023

Dosage forms

Dosage formProductsShare
Tablet, film coated2429.6%
Ointment2328.4%
Tablet, delayed release1417.3%
Gel44.9%
Tablet, coated44.9%
Suspension44.9%
Solution33.7%
Swab33.7%
Capsule, delayed release11.2%
Capsule, delayed release pellets11.2%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)7997.5%
Unapproved drugs for a shortage11.2%
Authorized generics (NDA)11.2%

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.