Data / Drug companies / Protease Inhibitor
Protease Inhibitor drugs: 12 drugs from 26 companies in the FDA NDC directory
Protease Inhibitor is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 77 products in this class from 26 companies, covering 12 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on February 27, 2026.
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- 26Companies
- 77Products
- 12Drugs by generic name
Drugs in the Protease Inhibitor class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Darunavir | 30 | 14 |
| Ritonavir | 9 | 8 |
| Atazanavir | 13 | 4 |
| Lopinavir and ritonavir | 9 | 4 |
| Darunavir ethanolate and cobicistat | 4 | 2 |
| Fosamprenavir calcium | 2 | 2 |
| Atazanavir sulfate | 3 | 1 |
| Nelfinavir mesylate | 2 | 1 |
| Atazanavir and cobicistat | 1 | 1 |
| Darunavir 600 mg | 1 | 1 |
| Darunavir 800 mg | 1 | 1 |
| Ritonavir 100 mg | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Camber Pharmaceuticals, Inc. | 10 | tablet, film coated; capsule | Generic drugs (ANDA) | January 21, 2025 |
| Janssen Products, LP | 9 | tablet, film coated; tablet, for suspension | New drug applications (NDA) | February 27, 2026 |
| AbbVie Inc. | 5 | tablet, film coated; solution | New drug applications (NDA) | August 16, 2022 |
| Aurobindo Pharma Limited | 5 | capsule; tablet, film coated | Generic drugs (ANDA) | September 17, 2018 |
| Laurus Labs Limited | 5 | capsule; tablet, film coated | Generic drugs (ANDA) | March 22, 2022 |
| E.r. Squibb & Sons, L.L.C. | 4 | capsule, gelatin coated; tablet | New drug applications (NDA) | January 29, 2015 |
| American Health Packaging | 3 | tablet; tablet, film coated | Generic drugs (ANDA) | June 25, 2024 |
| Cipla USA Inc. | 3 | tablet | Generic drugs (ANDA) | November 29, 2023 |
| Teva Pharmaceuticals USA, Inc. | 3 | capsule | Generic drugs (ANDA) | December 27, 2017 |
| Agouron | 2 | tablet, film coated | New drug applications (NDA) | April 30, 2003 |
| Amneal Pharmaceuticals NY LLC | 2 | tablet, film coated | Generic drugs (ANDA) | December 9, 2023 |
| Aurobindo Pharma Limited | 2 | tablet, film coated | Generic drugs (ANDA) | November 28, 2023 |
| Bryant Ranch Prepack | 2 | tablet | Generic drugs (ANDA) | November 29, 2023 |
| Bryant Ranch Prepack | 2 | tablet, film coated | Generic drugs (ANDA) | November 28, 2023 |
| Dr. Reddy's Laboratories Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | November 29, 2023 |
| Exelan Pharmaceuticals Inc. | 2 | tablet | Generic drugs (ANDA) | January 19, 2024 |
| Lupin Pharmaceuticals, Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | June 1, 2023 |
| Macleods Pharmaceuticals Limited | 2 | tablet, film coated | Generic drugs (ANDA) | July 25, 2024 |
| Novadoz Pharmaceuticals LLC | 2 | tablet, film coated | Generic drugs (ANDA) | November 28, 2023 |
| NuCare Pharmaceuticals,Inc. | 2 | tablet, film coated | Generic drugs (ANDA) | November 28, 2023 |
| Viona Pharmaceuticals Inc | 2 | tablet, film coated | Generic drugs (ANDA) | May 1, 2024 |
| Zydus Lifesciences Limited | 2 | tablet, film coated | Generic drugs (ANDA) | May 1, 2024 |
| A-S Medication Solutions | 1 | tablet, film coated | New drug applications (NDA) | January 31, 2015 |
| Amneal Pharmaceuticals LLC | 1 | tablet | Generic drugs (ANDA) | September 21, 2018 |
| Mylan Pharmaceuticals Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | September 18, 2017 |
| Sun Pharmaceutical Industries, Inc. | 1 | tablet, coated | Generic drugs (ANDA) | November 28, 2019 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 44 | 57.1% |
| Capsule | 13 | 16.9% |
| Tablet | 12 | 15.6% |
| Capsule, gelatin coated | 2 | 2.6% |
| Powder | 2 | 2.6% |
| Solution | 1 | 1.3% |
| Tablet, coated | 1 | 1.3% |
| Tablet, for suspension | 1 | 1.3% |
| Suspension | 1 | 1.3% |
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.