Skip to the page

Data / Drug companies / Monoamine Oxidase Inhibitor

Monoamine Oxidase Inhibitor drugs: 8 drugs from 37 companies in the FDA NDC directory

Monoamine Oxidase Inhibitor is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 60 products in this class from 37 companies, covering 8 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on October 20, 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.

  • 37Companies
  • 60Products
  • 8Drugs by generic name

Drugs in the Monoamine Oxidase Inhibitor class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Selegiline hydrochloride1412
Rasagiline2111
Rasagiline mesylate126
Phenelzine sulfate33
Tranylcypromine33
Tranylcypromine sulfate33
Selegiline31
Isocarboxazid11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Chartwell RX, LLC3tabletGeneric drugs (ANDA)July 27, 2018
Remedyrepack Inc.3tabletGeneric drugs (ANDA)August 25, 2026
Viatris Specialty LLC3patchNew drug applications (NDA)February 27, 2006
Alvogen Inc.2tabletGeneric drugs (ANDA)March 1, 2019
Ani Pharmaceuticals, Inc.2tablet; capsuleGeneric drugs (ANDA)June 6, 2021
Apotex Corp.2capsule; tabletGeneric drugs (ANDA)July 15, 1997
Ascend Laboratories, LLC2tabletGeneric drugs (ANDA)October 30, 2017
Aurobindo Pharma Limited2tabletGeneric drugs (ANDA)October 20, 2026
Bryant Ranch Prepack2capsuleGeneric drugs (ANDA)April 1, 2021
Carnegie Pharmaceuticals LLC2tabletGeneric drugs (ANDA)January 15, 2026
Florida Pharmaceutical Products, LLC2tabletGeneric drugs (ANDA)April 14, 2026
Golden State Medical Supply, Inc.2tabletGeneric drugs (ANDA)November 18, 2021
Macleods Pharmaceuticals Limited2tabletGeneric drugs (ANDA)June 29, 2024
Micro Labs Limited2tabletGeneric drugs (ANDA)April 3, 2019
NorthStar Rx LLC2tabletGeneric drugs (ANDA)April 17, 2018
Rising Pharma Holdings, Inc.2tabletGeneric drugs (ANDA)July 21, 2025
SKG Pharma Inc.2tabletGeneric drugs (ANDA)April 4, 2025
Teva Neuroscience, Inc.2tabletNew drug applications (NDA)July 10, 2006
Teva Pharmaceuticals USA, Inc.2tabletAuthorized generics (NDA)January 3, 2017
Torrent Pharmaceuticals Limited2tabletGeneric drugs (ANDA)November 15, 2025
A-S Medication Solutions1tabletGeneric drugs (ANDA)July 6, 1997
A2A Integrated Pharmaceuticals1tabletGeneric drugs (ANDA)March 15, 2024
Actavis Pharma, Inc.1tablet, film coatedAuthorized generics (NDA)February 5, 2016
Advanz Pharma (US) Corp.1tablet, film coatedNew drug applications (NDA)January 14, 2013
Bausch Health US LLC1tablet, orally disintegratingNew drug applications (NDA)June 14, 2006
Bryant Ranch Prepack1tabletGeneric drugs (ANDA)April 3, 2019
Golden State Medical Supply, Inc.1tabletGeneric drugs (ANDA)June 6, 1997
I3 Pharmaceuticals, LLC1tabletGeneric drugs (ANDA)December 15, 2021
Lifsa Drugs LLC1tabletNew drug applications (NDA)July 1, 1959
Lupin Pharmaceuticals,Inc.1tabletGeneric drugs (ANDA)December 14, 2010
Marlex Pharmaceuticals, Inc.1capsuleGeneric drugs (ANDA)May 1, 2021
Mylan Pharmaceuticals Inc.1tablet, film coatedAuthorized generics (NDA)March 23, 2011
Parke-Davis Div of Pfizer Inc1tablet, film coatedNew drug applications (NDA)June 9, 1961
Proficient Rx LP1capsuleGeneric drugs (ANDA)April 2, 2019
Rising Pharma Holdings, Inc.1capsuleGeneric drugs (ANDA)April 2, 2019
Solco Healthcare US, LLC1tabletGeneric drugs (ANDA)December 10, 2022
Strides Pharma Science Limited1tablet, film coatedGeneric drugs (ANDA)April 11, 2022

Dosage forms

Dosage formProductsShare
Tablet4473.3%
Capsule711.7%
Tablet, film coated58.3%
Patch35%
Tablet, orally disintegrating11.7%

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.