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.
| Drug | Products here | Companies listing it |
|---|---|---|
| Valganciclovir | 12 | 14 |
| Valganciclovir hydrochloride | 14 | 11 |
| Ganciclovir sodium | 7 | 5 |
| Ribavirin | 3 | 2 |
| Ganciclovir | 2 | 2 |
| Ribavirinum | 8 | 1 |
| Trifluridine and tipiracil | 2 | 1 |
| Trifluridine | 1 | 1 |
| Valganciclovir hydrochloride powder, | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Hahnemann Laboratories, Inc. | 8 | pellet | Unapproved homeopathic products | October 12, 2023 |
| Aurobindo Pharma Limited | 3 | capsule; tablet | Generic drugs (ANDA) | March 31, 2016 |
| Ajanta Pharma USA Inc. | 2 | tablet; powder, for solution | Generic drugs (ANDA) | January 13, 2020 |
| AvKARE | 2 | powder, for solution; tablet, film coated | Generic drugs (ANDA) | December 21, 2023 |
| Camber Pharmaceuticals, Inc. | 2 | tablet, film coated; powder, for solution | Generic drugs (ANDA) | October 4, 2022 |
| Fresenius Kabi USA, LLC | 2 | injection, powder, lyophilized, for solution | Generic drugs (ANDA) | June 28, 2010 |
| H2-Pharma, LLC | 2 | tablet, film coated; powder, for solution | New drug applications (NDA) | August 28, 2009 |
| NorthStar RxLLC | 2 | powder, for solution; tablet | Generic drugs (ANDA) | March 1, 2026 |
| Slate Run Pharmaceuticals, LLC | 2 | injection, powder, lyophilized, for solution | Generic drugs (ANDA) | January 1, 2019 |
| Strides Pharma Science Limited | 2 | tablet, film coated | Generic drugs (ANDA) | June 16, 2025 |
| Taiho Pharmaceutical Co., LTD. | 2 | tablet, film coated | New drug applications (NDA) | September 22, 2015 |
| Actavis Pharma, Inc. | 1 | powder, for solution | Generic drugs (ANDA) | August 26, 2016 |
| Airis Pharma PVT LTD | 1 | for solution | Generic drugs (ANDA) | February 28, 2022 |
| Alembic Pharmaceuticals Inc. | 1 | powder, for solution | Generic drugs (ANDA) | October 28, 2026 |
| Alembic Pharmaceuticals Limited | 1 | powder, for solution | Generic drugs (ANDA) | October 28, 2026 |
| American Health Packaging | 1 | tablet, film coated | Generic drugs (ANDA) | January 16, 2015 |
| American Health Packaging | 1 | powder, for solution | Generic drugs (ANDA) | August 20, 2023 |
| Aurobindo Pharma Limited | 1 | for solution | Generic drugs (ANDA) | November 17, 2022 |
| AvPAK | 1 | tablet, film coated | Generic drugs (ANDA) | July 27, 2016 |
| Bausch & Lomb Incorporated | 1 | gel | New drug applications (NDA) | April 30, 2010 |
| Dr. Reddy's Laboratories Inc. | 1 | tablet | Generic drugs (ANDA) | December 12, 2017 |
| Dr. Reddy's Laboratories Limited | 1 | tablet, film coated | Generic drugs (ANDA) | December 15, 2014 |
| Florida Pharmaceutical Products, LLC | 1 | powder, for solution | Generic drugs (ANDA) | July 1, 2023 |
| Hikma Pharmaceuticals USA Inc. | 1 | injection, powder, lyophilized, for solution | Generic drugs (ANDA) | June 17, 2021 |
| Major Pharmaceuticals | 1 | tablet, film coated | Generic drugs (ANDA) | March 18, 2016 |
| Micro Labs Limited | 1 | powder, for solution | Generic drugs (ANDA) | June 1, 2026 |
| Novadoz Pharmaceuticals LLC | 1 | for solution | Generic drugs (ANDA) | February 17, 2022 |
| Oceanside Pharmaceuticals | 1 | powder, for solution | New drug applications (NDA) | April 14, 2017 |
| Par Health USA, LLC | 1 | injection, powder, lyophilized, for solution | Generic drugs (ANDA) | December 6, 2016 |
| Pharmascience Inc. | 1 | injection, solution | Generic drugs (ANDA) | April 24, 2018 |
| Sagent Pharmaceuticals | 1 | injection, solution | Generic drugs (ANDA) | February 15, 2018 |
| Sandoz Inc | 1 | solution | Generic drugs (ANDA) | May 14, 2001 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 12 | 24% |
| Powder, for solution | 12 | 24% |
| Pellet | 8 | 16% |
| Injection, powder, lyophilized, for solution | 6 | 12% |
| Tablet | 4 | 8% |
| For solution | 3 | 6% |
| Injection, solution | 2 | 4% |
| Capsule | 1 | 2% |
| Solution | 1 | 2% |
| Gel | 1 | 2% |
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.