Data / Drug companies / Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor
Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor drugs: 13 drugs from 24 companies in the FDA NDC directory
Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 56 products in this class from 24 companies, covering 13 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on July 10, 2026.
SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.
- 24Companies
- 56Products
- 13Drugs by generic name
Drugs in the Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Etravirine | 16 | 7 |
| Efavirenz, emtricitabine and tenofovir disoproxil fumarate | 7 | 7 |
| Nevirapine | 9 | 6 |
| Efavirenz | 8 | 5 |
| Efavirenz, lamivudine and tenofovir disoproxil fumarate | 3 | 2 |
| Doravirine | 2 | 2 |
| Rilpivirine | 2 | 2 |
| Rilpivirine hydrochloride | 2 | 1 |
| Dolutegravir sodium and rilpivirine hydrochloride | 1 | 1 |
| Doravirine, islatravir | 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 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Aurobindo Pharma Limited | 7 | capsule; tablet, film coated | Generic drugs (ANDA) | March 30, 2021 |
| Janssen Products, LP | 5 | tablet; tablet, film coated | New drug applications (NDA) | March 15, 2024 |
| Laurus Labs Limited | 5 | tablet, film coated | Generic drugs (ANDA) | July 10, 2026 |
| Macleods Pharmaceuticals Limited | 4 | tablet; tablet, extended release | Generic drugs (ANDA) | May 10, 2024 |
| Amneal Pharmaceuticals NY LLC | 3 | tablet | Generic drugs (ANDA) | June 14, 2021 |
| Camber Pharmaceuticals, Inc. | 3 | tablet, film coated; tablet | Generic drugs (ANDA) | January 24, 2022 |
| Merck Sharp & Dohme LLC | 3 | tablet, film coated | New drug applications (NDA) | April 23, 2026 |
| Mylan Pharmaceuticals Inc. | 3 | tablet, film coated; tablet | Generic drugs (ANDA) | May 27, 2025 |
| AvKARE | 2 | tablet | Generic drugs (ANDA) | October 4, 2022 |
| Bionpharma Inc. | 2 | tablet | Generic drugs (ANDA) | January 1, 2026 |
| Carnegie Pharmaceuticals LLC | 2 | tablet | Generic drugs (ANDA) | June 7, 2022 |
| Cipla USA Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | March 30, 2021 |
| Gilead Sciences, Inc. | 2 | tablet; tablet, film coated | New drug applications (NDA) | March 1, 2016 |
| Leading Pharma, LLC | 2 | tablet | Generic drugs (ANDA) | June 5, 2022 |
| Patriot Pharmaceuticals | 2 | tablet | New drug applications (NDA) | April 1, 2025 |
| A-S Medication Solutions | 1 | tablet, film coated | New drug applications (NDA) | July 20, 2018 |
| Amneal Pharmaceuticals LLC | 1 | tablet | Generic drugs (ANDA) | April 30, 2014 |
| Bryant Ranch Prepack | 1 | tablet, film coated | Generic drugs (ANDA) | March 30, 2021 |
| Micro Labs Limited | 1 | tablet | Generic drugs (ANDA) | May 22, 2012 |
| Somerset Therapeutics, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | January 30, 2026 |
| Teva Pharmaceuticals USA, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | October 1, 2020 |
| Viatris Specialty LLC | 1 | tablet, film coated | New drug applications (NDA) | April 25, 2018 |
| ViiV Healthcare Company | 1 | tablet, film coated | New drug applications (NDA) | November 21, 2017 |
| XLCare Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | May 29, 2021 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 25 | 44.6% |
| Tablet | 24 | 42.9% |
| Capsule | 3 | 5.4% |
| Tablet, extended release | 2 | 3.6% |
| Tablet, for suspension | 1 | 1.8% |
| Suspension | 1 | 1.8% |
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.