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Data / Drug companies / Antiprotozoal

Antiprotozoal drugs: 8 drugs from 35 companies in the FDA NDC directory

Antiprotozoal is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 51 products in this class from 35 companies, covering 8 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on June 14, 2026.

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  • 35Companies
  • 51Products
  • 8Drugs by generic name

Drugs in the Antiprotozoal class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Atovaquone2319
Atovaquone and proguanil hydrochloride129
Pentamidine isethionate85
Nitazoxanide44
Atovaquone and proguanil hydrochloride pediatric11
Atovaquone oral suspension11
Eflornithine hydrochloride11
Paromomycin sulfate11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
GlaxoSmithKline LLC4suspension; tablet, film coatedNew drug applications (NDA)July 26, 2000
Pai Holdings, LLC DBA Pai Pharma4suspension; injection, powder, lyophilized, for solutionGeneric drugs (ANDA)June 12, 2026
Glenmark Pharmaceuticals Inc., USA3tablet, film coated; suspensionGeneric drugs (ANDA)December 31, 2017
A-S Medication Solutions2tablet, film coatedAuthorized generics (NDA)July 27, 2012
Atlantic Biologicals Corp.2suspensionGeneric drugs (ANDA)October 11, 2018
Camber Pharmaceuticals, Inc.2suspension; tablet, film coatedGeneric drugs (ANDA)April 15, 2025
Fresenius Kabi USA, LLC2injection, powder, lyophilized, for solution; inhalantNew drug applications (NDA)February 15, 2011
Golden State Medical Supply, Inc.2tablet, film coated; suspensionGeneric drugs (ANDA)March 30, 2021
Kesin Pharma Corporation2suspensionGeneric drugs (ANDA)February 6, 2026
Mylan Pharmaceuticals Inc.2tablet, film coatedGeneric drugs (ANDA)May 28, 2014
Seton Pharmaceuticals2injection, powder, lyophilized, for solution; inhalantGeneric drugs (ANDA)October 14, 2019
Abon Pharmaceuticals, LLC1suspensionGeneric drugs (ANDA)November 14, 2023
American Health Packaging1suspensionGeneric drugs (ANDA)October 21, 2020
Amneal Pharmaceuticals LLC1suspensionGeneric drugs (ANDA)February 9, 2011
Ani Pharmaceuticals, Inc.1tabletGeneric drugs (ANDA)March 5, 2025
AvKARE1suspensionGeneric drugs (ANDA)June 14, 2026
AvPAK1suspensionGeneric drugs (ANDA)October 14, 2025
Bionpharma Inc.1suspensionGeneric drugs (ANDA)June 1, 2021
BluePoint Laboratories1tablet, film coatedGeneric drugs (ANDA)March 13, 2014
Bryant Ranch Prepack1tablet, film coatedGeneric drugs (ANDA)September 15, 2011
Chartwell Governmental & Specialty RX, LLC.1suspensionGeneric drugs (ANDA)April 28, 2017
Chartwell RX, LLC1suspensionGeneric drugs (ANDA)April 28, 2017
E5 Pharma, LLC1tabletGeneric drugs (ANDA)June 1, 2026
Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)January 8, 2021
KVK-Tech, Inc.1suspensionGeneric drugs (ANDA)March 29, 2019
Lohxa1suspensionGeneric drugs (ANDA)October 11, 2018
Lupin Pharmaceuticals, Inc.1suspensionGeneric drugs (ANDA)June 1, 2021
Major Pharmaceuticals1suspensionGeneric drugs (ANDA)July 8, 2024
NorthStar RxLLC1suspensionGeneric drugs (ANDA)May 1, 2024
Prasco Laboratories1tablet, film coatedAuthorized generics (NDA)July 27, 2012
Proficient Rx LP1tablet, film coatedGeneric drugs (ANDA)August 18, 2011
Rising Pharma Holdings, Inc.1tablet, film coatedGeneric drugs (ANDA)November 27, 2020
Uswm, LLC1tabletNew drug applications (NDA)January 15, 2024
Waylis Therapeutics LLC1capsuleGeneric drugs (ANDA)April 8, 2021
XGen Pharmaceuticals DJB, Inc.1inhalantGeneric drugs (ANDA)April 4, 2023

Dosage forms

Dosage formProductsShare
Suspension2447.1%
Tablet, film coated1529.4%
Injection, powder, lyophilized, for solution47.8%
Inhalant47.8%
Tablet35.9%
Capsule12%

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.