Data / Drug companies / Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor
Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor drugs: 22 drugs from 58 companies in the FDA NDC directory
Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 182 products in this class from 58 companies, covering 22 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on March 5, 2026.
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- 58Companies
- 182Products
- 22Drugs by generic name
Drugs in the Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Emtricitabine and tenofovir disoproxil fumarate | 48 | 28 |
| Tenofovir disoproxil fumarate | 25 | 16 |
| Entecavir | 29 | 15 |
| Lamivudine | 27 | 14 |
| Lamivudine and zidovudine | 10 | 8 |
| Efavirenz, emtricitabine and tenofovir disoproxil fumarate | 7 | 7 |
| Abacavir and lamivudine | 6 | 6 |
| Efavirenz, lamivudine and tenofovir disoproxil fumarate | 3 | 2 |
| Adefovir dipivoxil | 2 | 2 |
| Lamivudine oral | 2 | 2 |
| Emtricitabine and tenofovir alafenamide | 2 | 1 |
| Entecavir anhydrous | 2 | 1 |
| Abacavir , lamivudine and zidovudine | 1 | 1 |
| Abacavir sulfate, dolutegravir sodium, lamivudine | 1 | 1 |
| Dolutegravir sodium and lamivudine | 1 | 1 |
| Doravirine, lamivudine, and tenofovir disoproxil fumarate | 1 | 1 |
| Emtricitabine, rilpivirine and tenofovir disoproxil fumarate | 1 | 1 |
| Emtricitabine, rilpivirine, tenofovir disoproxil fumarate | 1 | 1 |
| Emtricitabine/tdf | 1 | 1 |
| Lamivudine and tenofovir disoproxil fumarate | 1 | 1 |
| Tenofovir alafenamide | 1 | 1 |
| Tenofovir disoproxil fumarate tablets | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Gilead Sciences, Inc. | 19 | tablet; tablet, film coated | New drug applications (NDA) | October 8, 2024 |
| Aurobindo Pharma Limited | 13 | tablet, film coated; tablet | Generic drugs (ANDA) | March 30, 2021 |
| Camber Pharmaceuticals, Inc. | 12 | tablet, film coated; tablet | Generic drugs (ANDA) | April 16, 2025 |
| Cipla USA Inc. | 7 | tablet, film coated; tablet | Generic drugs (ANDA) | November 1, 2021 |
| Macleods Pharmaceuticals Limited | 7 | tablet, film coated; tablet | Generic drugs (ANDA) | December 20, 2024 |
| A-S Medication Solutions | 6 | tablet, film coated; tablet, coated | Generic drugs (ANDA) | November 26, 2025 |
| Laurus Labs Limited | 6 | tablet, film coated | Generic drugs (ANDA) | March 5, 2026 |
| ViiV Healthcare Company | 6 | tablet, film coated; solution | New drug applications (NDA) | April 8, 2019 |
| Zydus Lifesciences Limited | 6 | tablet, film coated | Generic drugs (ANDA) | July 1, 2021 |
| Bryant Ranch Prepack | 5 | tablet, film coated; tablet, coated | Generic drugs (ANDA) | November 26, 2025 |
| Amneal Pharmaceuticals NY LLC | 4 | tablet, film coated | Generic drugs (ANDA) | August 26, 2018 |
| Apotex Corp. | 4 | tablet, film coated; tablet | Generic drugs (ANDA) | September 25, 2018 |
| Epic Pharma, LLC | 4 | tablet; tablet, film coated | Generic drugs (ANDA) | October 31, 2022 |
| Lupin Pharmaceuticals, Inc. | 4 | tablet, film coated; tablet | Generic drugs (ANDA) | June 23, 2021 |
| NorthStar Rx LLC | 4 | tablet, film coated | Generic drugs (ANDA) | March 9, 2022 |
| NuCare Pharmaceuticals,Inc. | 4 | tablet, film coated | Generic drugs (ANDA) | March 9, 2022 |
| Strides Pharma Science Limited | 4 | tablet; tablet, film coated | Generic drugs (ANDA) | March 30, 2021 |
| Zydus Pharmaceuticals USA Inc. | 4 | tablet, film coated | Generic drugs (ANDA) | July 1, 2021 |
| Aurobindo Pharma Limited | 3 | tablet, film coated | Generic drugs (ANDA) | March 9, 2023 |
| AvKARE | 3 | tablet, film coated | Generic drugs (ANDA) | July 1, 2025 |
| E.r. Squibb & Sons, L.L.C. | 3 | tablet, film coated; solution | New drug applications (NDA) | March 29, 2005 |
| Golden State Medical Supply, Inc. | 3 | tablet; tablet, film coated | Generic drugs (ANDA) | November 10, 2021 |
| Major Pharmaceuticals | 3 | tablet, film coated | Generic drugs (ANDA) | July 26, 2019 |
| American Health Packaging | 2 | tablet; tablet, film coated | Generic drugs (ANDA) | January 19, 2023 |
| Amneal Pharmaceuticals LLC | 2 | tablet, film coated | Generic drugs (ANDA) | November 28, 2014 |
| Cameron Pharmaceuticals | 2 | tablet | Generic drugs (ANDA) | May 15, 2025 |
| Chartwell RX, LLC | 2 | tablet, film coated; solution | Generic drugs (ANDA) | July 31, 2018 |
| Direct_Rx | 2 | tablet, film coated | Generic drugs (ANDA) | December 5, 2022 |
| Exelan Pharmaceuticals Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | April 6, 2021 |
| Golden State Medical Supply, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | December 2, 2011 |
| Ingenus Pharmaceuticals, LLC | 2 | tablet | Generic drugs (ANDA) | February 1, 2017 |
| Solco Healthcare US, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | April 1, 2018 |
| Teva Pharmaceuticals USA, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | January 20, 2021 |
| Viatris Specialty LLC | 2 | tablet, film coated | New drug applications (NDA) | June 25, 2018 |
| Yaopharma Co., Ltd. | 2 | tablet, film coated | Generic drugs (ANDA) | July 1, 2023 |
| Zydus Pharmaceuticals USA Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | August 10, 2017 |
| Amneal Pharmaceuticals NY LLC | 1 | tablet, film coated | Generic drugs (ANDA) | August 26, 2018 |
| AvPAK | 1 | tablet | Generic drugs (ANDA) | March 30, 2020 |
| Bryant Ranch Prepack | 1 | tablet, film coated | Generic drugs (ANDA) | March 30, 2021 |
| Bryant Ranch Prepack | 1 | tablet, film coated | Generic drugs (ANDA) | January 26, 2018 |
| Carlsbad Technology, Inc. | 1 | tablet | Generic drugs (ANDA) | November 10, 2021 |
| Chartwell Governmental & Specialty RX, LLC. | 1 | solution | Generic drugs (ANDA) | October 31, 2014 |
| Coupler LLC | 1 | tablet, film coated | Generic drugs (ANDA) | February 6, 2025 |
| Florida Pharmaceutical Products, LLC | 1 | tablet, coated | Generic drugs (ANDA) | November 26, 2025 |
| Janssen Products, LP | 1 | tablet, film coated | New drug applications (NDA) | July 17, 2018 |
| Merck Sharp & Dohme LLC | 1 | tablet, film coated | New drug applications (NDA) | July 20, 2018 |
| Mylan Pharmaceuticals Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | May 27, 2025 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | September 18, 2015 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | October 26, 2023 |
| Proficient Rx LP | 1 | tablet, film coated | Generic drugs (ANDA) | October 7, 2021 |
| Proficient Rx LP | 1 | tablet, film coated | Generic drugs (ANDA) | March 30, 2021 |
| Quallent Pharmaceuticals Health LLC | 1 | tablet, film coated | Generic drugs (ANDA) | September 1, 2023 |
| Quinn Pharmaceuticals | 1 | tablet, coated | Generic drugs (ANDA) | January 1, 2020 |
| Redpharm Drug | 1 | tablet, film coated | Generic drugs (ANDA) | October 7, 2021 |
| Rising Pharma Holdings, Inc. | 1 | solution | Generic drugs (ANDA) | November 21, 2016 |
| Sigmapharm Laboratories, LLC | 1 | tablet | Generic drugs (ANDA) | September 3, 2013 |
| Strides Pharma Inc. | 1 | tablet | Generic drugs (ANDA) | March 30, 2021 |
| XLCare Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | April 17, 2020 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 133 | 73.1% |
| Tablet | 33 | 18.1% |
| Tablet, coated | 9 | 4.9% |
| Solution | 6 | 3.3% |
| Powder | 1 | 0.5% |
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.