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Data / Drug companies / Nucleoside Analog Antiviral

Nucleoside Analog Antiviral drugs: 9 drugs from 32 companies in the FDA NDC directory

Nucleoside Analog Antiviral is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 50 products in this class from 32 companies, covering 9 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on October 28, 2026.

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  • 32Companies
  • 50Products
  • 9Drugs by generic name

Drugs in the Nucleoside Analog Antiviral class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Valganciclovir1214
Valganciclovir hydrochloride1411
Ganciclovir sodium75
Ribavirin32
Ganciclovir22
Ribavirinum81
Trifluridine and tipiracil21
Trifluridine11
Valganciclovir hydrochloride powder,11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Hahnemann Laboratories, Inc.8pelletUnapproved homeopathic productsOctober 12, 2023
Aurobindo Pharma Limited3capsule; tabletGeneric drugs (ANDA)March 31, 2016
Ajanta Pharma USA Inc.2tablet; powder, for solutionGeneric drugs (ANDA)January 13, 2020
AvKARE2powder, for solution; tablet, film coatedGeneric drugs (ANDA)December 21, 2023
Camber Pharmaceuticals, Inc.2tablet, film coated; powder, for solutionGeneric drugs (ANDA)October 4, 2022
Fresenius Kabi USA, LLC2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)June 28, 2010
H2-Pharma, LLC2tablet, film coated; powder, for solutionNew drug applications (NDA)August 28, 2009
NorthStar RxLLC2powder, for solution; tabletGeneric drugs (ANDA)March 1, 2026
Slate Run Pharmaceuticals, LLC2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)January 1, 2019
Strides Pharma Science Limited2tablet, film coatedGeneric drugs (ANDA)June 16, 2025
Taiho Pharmaceutical Co., LTD.2tablet, film coatedNew drug applications (NDA)September 22, 2015
Actavis Pharma, Inc.1powder, for solutionGeneric drugs (ANDA)August 26, 2016
Airis Pharma PVT LTD1for solutionGeneric drugs (ANDA)February 28, 2022
Alembic Pharmaceuticals Inc.1powder, for solutionGeneric drugs (ANDA)October 28, 2026
Alembic Pharmaceuticals Limited1powder, for solutionGeneric drugs (ANDA)October 28, 2026
American Health Packaging1tablet, film coatedGeneric drugs (ANDA)January 16, 2015
American Health Packaging1powder, for solutionGeneric drugs (ANDA)August 20, 2023
Aurobindo Pharma Limited1for solutionGeneric drugs (ANDA)November 17, 2022
AvPAK1tablet, film coatedGeneric drugs (ANDA)July 27, 2016
Bausch & Lomb Incorporated1gelNew drug applications (NDA)April 30, 2010
Dr. Reddy's Laboratories Inc.1tabletGeneric drugs (ANDA)December 12, 2017
Dr. Reddy's Laboratories Limited1tablet, film coatedGeneric drugs (ANDA)December 15, 2014
Florida Pharmaceutical Products, LLC1powder, for solutionGeneric drugs (ANDA)July 1, 2023
Hikma Pharmaceuticals USA Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)June 17, 2021
Major Pharmaceuticals1tablet, film coatedGeneric drugs (ANDA)March 18, 2016
Micro Labs Limited1powder, for solutionGeneric drugs (ANDA)June 1, 2026
Novadoz Pharmaceuticals LLC1for solutionGeneric drugs (ANDA)February 17, 2022
Oceanside Pharmaceuticals1powder, for solutionNew drug applications (NDA)April 14, 2017
Par Health USA, LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)December 6, 2016
Pharmascience Inc.1injection, solutionGeneric drugs (ANDA)April 24, 2018
Sagent Pharmaceuticals1injection, solutionGeneric drugs (ANDA)February 15, 2018
Sandoz Inc1solutionGeneric drugs (ANDA)May 14, 2001

Dosage forms

Dosage formProductsShare
Tablet, film coated1224%
Powder, for solution1224%
Pellet816%
Injection, powder, lyophilized, for solution612%
Tablet48%
For solution36%
Injection, solution24%
Capsule12%
Solution12%
Gel12%

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.