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Data / Drug companies / Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor

Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor drugs: 7 drugs from 32 companies in the FDA NDC directory

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

Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 40 products in this class from 32 companies, covering 7 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
  • 40Products
  • 7Drugs by generic name

Drugs in the Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor class

Ranked by number of companies that list the drug.

DrugProducts hereCompanies listing it
Valganciclovir1414
Valganciclovir hydrochloride1411
Ganciclovir sodium75
Ganciclovir22
Cidofovir anhydrous11
Cidofovir dihydrate11
Valganciclovir hydrochloride powder,11

Companies with the most products in this class

CompanyProductsMain dosage formsMain marketing categoryNewest product started
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
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 Limited1tabletGeneric drugs (ANDA)March 31, 2016
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
Granules Pharmaceuticals Inc.1for solutionGeneric drugs (ANDA)July 1, 2021
Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc.1injection, solutionGeneric drugs (ANDA)August 6, 2012
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
Mylan Institutional LLC1injection, solutionGeneric drugs (ANDA)June 3, 2013
Novadoz Pharmaceuticals LLC1for solutionGeneric drugs (ANDA)February 17, 2022
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
Somerset Therapeutics, LLC1for solutionGeneric drugs (ANDA)January 15, 2022

Dosage forms

Dosage formProductsShare
Powder, for solution1127.5%
Tablet, film coated922.5%
Injection, powder, lyophilized, for solution615%
For solution512.5%
Injection, solution410%
Tablet410%
Gel12.5%

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.