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Data / Drug companies / Substance P/Neurokinin-1 Receptor Antagonist

Substance P/Neurokinin-1 Receptor Antagonist drugs: 5 drugs from 29 companies in the FDA NDC directory

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

Substance P/Neurokinin-1 Receptor Antagonist is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 52 products in this class from 29 companies, covering 5 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on October 20, 2026.

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  • 29Companies
  • 52Products
  • 5Drugs by generic name

Drugs in the Substance P/Neurokinin-1 Receptor Antagonist class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Fosaprepitant dimeglumine1312
Fosaprepitant1410
Aprepitant227
Rolapitant22
Netupitant and palonosetron11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
BluePoint Laboratories6capsule; injection, powder, lyophilized, for solutionGeneric drugs (ANDA)February 10, 2026
Merck Sharp & Dohme LLC5capsule; injection, powder, lyophilized, for solutionNew drug applications (NDA)February 3, 2017
Torrent Pharmaceuticals Limited4capsuleGeneric drugs (ANDA)October 20, 2026
Dr. Reddy's Laboratories Inc.3injection, powder, lyophilized, for solutionGeneric drugs (ANDA)February 12, 2026
Glenmark Pharmaceuticals Inc., USA3capsuleGeneric drugs (ANDA)October 12, 2017
Golden State Medical Supply, Inc.3capsuleGeneric drugs (ANDA)October 21, 2020
Sandoz Inc3capsuleGeneric drugs (ANDA)December 27, 2016
Heron Therapeutics, Inc.2emulsion; injection, emulsionNew drug applications (NDA)March 6, 2023
Hikma Pharmaceuticals USA Inc.2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 1, 2021
Novadoz Pharmaceuticals LLC2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 12, 2020
Actavis Pharma, Inc.1injection, powder, lyophilized, for solutionNew drug applications (NDA)September 19, 2019
Amneal Pharmaceuticals LLC1injectionNew drug applications (NDA)June 1, 2024
Avenacy, LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)February 28, 2024
Avyxa Pharma, LLC1injection, powder, lyophilized, for solutionNew drug applications (NDA)July 23, 2026
Baxter Healthcare Corporation1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)September 5, 2019
Be Pharmaceuticals Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)October 15, 2019
Bryant Ranch Prepack1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 12, 2020
Camber Pharmaceuticals, Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)July 29, 2021
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)March 16, 2021
Eugia US LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)January 12, 2021
Fresenius Kabi USA, LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)September 5, 2019
Helsinn Therapeutics (U.S.), Inc.1capsuleNew drug applications (NDA)October 13, 2014
Luria Therapeutics LLC1tabletNew drug applications (NDA)August 20, 2026
Mylan Institutional LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)September 5, 2019
NorthStar Rx LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)January 28, 2023
NorthStar RxLLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)September 5, 2019
Qilu Pharmaceutical Co., Ltd.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)September 8, 2020
Steriscience Specialties Private Limited1injectionNew drug applications (NDA)June 26, 2024
TerSera Therapeutics LLC1tabletNew drug applications (NDA)October 7, 2015

Dosage forms

Dosage formProductsShare
Injection, powder, lyophilized, for solution2548.1%
Capsule2038.5%
Tablet23.8%
Injection23.8%
Emulsion11.9%
Powder, for suspension11.9%
Injection, emulsion11.9%

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.