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Data / Drug companies / mTOR Inhibitor Immunosuppressant

mTOR Inhibitor Immunosuppressant drugs: 3 drugs from 35 companies in the FDA NDC directory

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

mTOR Inhibitor Immunosuppressant is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 125 products in this class from 35 companies, covering 3 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on October 27, 2026.

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  • 35Companies
  • 125Products
  • 3Drugs by generic name

Drugs in the mTOR Inhibitor Immunosuppressant class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Sirolimus4022
Everolimus8115
Everolimus tablets41

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Biocon Pharma Inc.11tablet; tablet, for suspensionGeneric drugs (ANDA)January 14, 2026
Breckenridge Pharmaceutical, Inc.11tablet; tablet, for suspensionGeneric drugs (ANDA)October 30, 2025
Novartis Pharmaceuticals Corporation11tablet; tablet, for suspensionNew drug applications (NDA)August 29, 2012
Hikma Pharmaceuticals USA Inc.8tabletGeneric drugs (ANDA)November 18, 2021
Natco Pharma Limited8tabletGeneric drugs (ANDA)October 1, 2021
Ascend Laboratories, LLC7tablet; tablet, film coatedGeneric drugs (ANDA)November 27, 2021
NorthStar RxLLC5tablet; solutionGeneric drugs (ANDA)October 1, 2024
Aurobindo Pharma Limited4tabletGeneric drugs (ANDA)February 25, 2026
CivicaScript LLC4tabletGeneric drugs (ANDA)March 5, 2021
I3 Pharmaceuticals, LLC4tabletGeneric drugs (ANDA)August 7, 2026
Mylan Pharmaceuticals Inc.4tablet, sugar coated; solutionAuthorized generics (NDA)July 22, 2019
Novugen Pharma (USA) LLC4tabletGeneric drugs (ANDA)March 30, 2026
Remedyrepack Inc.4tablet; tablet, film coatedGeneric drugs (ANDA)August 19, 2025
Upsher-Smith Laboratories, LLC4tabletGeneric drugs (ANDA)October 1, 2021
Amneal Pharmaceuticals NY LLC3tablet, for suspensionGeneric drugs (ANDA)January 14, 2025
Ani Pharmaceuticals, Inc.3tablet, for suspensionGeneric drugs (ANDA)October 10, 2025
Glenmark Pharmaceuticals Inc., USA3tablet, film coatedGeneric drugs (ANDA)October 16, 2020
NorthStar Rx LLC3tablet, film coatedGeneric drugs (ANDA)October 18, 2021
Zydus Lifesciences Limited3tablet, film coatedGeneric drugs (ANDA)February 16, 2023
Zydus Pharmaceuticals USA Inc.3tablet, film coatedGeneric drugs (ANDA)February 16, 2023
AvPAK2tablet; tablet, film coatedGeneric drugs (ANDA)October 27, 2026
Dr. Reddy's Laboratories Limited2tabletGeneric drugs (ANDA)October 27, 2014
Par Health USA, LLC2tabletGeneric drugs (ANDA)March 31, 2022
Aadi Bioscience, Inc.1injection, powder, lyophilized, for suspensionNew drug applications (NDA)December 6, 2021
American Health Packaging1tabletGeneric drugs (ANDA)November 5, 2015
American Health Packaging1tablet, film coatedGeneric drugs (ANDA)June 2, 2026
Amneal Pharmaceuticals NY LLC1solutionGeneric drugs (ANDA)October 25, 2019
Apotex Corp.1solutionGeneric drugs (ANDA)May 20, 2020
Bryant Ranch Prepack1solutionGeneric drugs (ANDA)January 19, 2023
Camber Pharmaceuticals, Inc.1solutionGeneric drugs (ANDA)September 16, 2024
Major Pharmaceuticals1tablet, film coatedGeneric drugs (ANDA)March 13, 2021
Nobelpharma America, LLC1gelNew drug applications (NDA)March 23, 2022
Novadoz Pharmaceuticals LLC1solutionGeneric drugs (ANDA)January 19, 2023
Rising Pharma Holdings, Inc.1solutionGeneric drugs (ANDA)July 15, 2025
VistaPharm, LLC1solutionGeneric drugs (ANDA)January 28, 2019

Dosage forms

Dosage formProductsShare
Tablet7660.8%
Tablet, film coated2016%
Tablet, for suspension1512%
Solution97.2%
Tablet, sugar coated32.4%
Gel10.8%
Injection, powder, lyophilized, for suspension10.8%

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.