Data / Drug companies / Neprilysin Inhibitor
Neprilysin Inhibitor drugs: 1 drug from 29 companies in the FDA NDC directory
Neprilysin Inhibitor is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 103 products in this class from 29 companies, covering 1 drug by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on October 26, 2026.
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- 29Companies
- 103Products
- 1Drugs by generic name
Drugs in the Neprilysin Inhibitor class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Sacubitril and valsartan | 103 | 29 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Aphena Pharma Solutions - Tennessee, LLC | 9 | tablet, film coated; tablet | Generic drugs (ANDA) | September 30, 2025 |
| Novartis Pharmaceuticals Corporation | 7 | tablet, film coated; pellet | New drug applications (NDA) | April 12, 2024 |
| AvKARE | 6 | tablet, film coated | Generic drugs (ANDA) | November 16, 2025 |
| Ascend Laboratories, LLC | 5 | tablet, film coated | Generic drugs (ANDA) | July 23, 2025 |
| Torrent Pharmaceuticals Limited | 5 | tablet | Generic drugs (ANDA) | July 16, 2025 |
| Novugen Pharma (USA) LLC | 4 | tablet, film coated | Generic drugs (ANDA) | July 16, 2025 |
| Alembic Pharmaceuticals Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | November 4, 2024 |
| Alembic Pharmaceuticals Limited | 3 | tablet, film coated | Generic drugs (ANDA) | November 4, 2024 |
| American Health Packaging | 3 | tablet, film coated | Generic drugs (ANDA) | June 11, 2026 |
| Amneal Pharmaceuticals NY LLC | 3 | tablet, film coated | Generic drugs (ANDA) | June 2, 2025 |
| Ani Pharmaceuticals, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | July 24, 2025 |
| Aurobindo Pharma Limited | 3 | tablet, film coated | Generic drugs (ANDA) | October 26, 2026 |
| AvPAK | 3 | tablet, film coated | Generic drugs (ANDA) | October 13, 2025 |
| Biocon Pharma Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | July 17, 2025 |
| Camber Pharmaceuticals, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | July 23, 2025 |
| Dr. Reddy's Laboratories Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | July 16, 2025 |
| Golden State Medical Supply, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | June 11, 2026 |
| Laurus Labs Limited | 3 | tablet, film coated | Generic drugs (ANDA) | November 11, 2024 |
| Lupin Pharmaceuticals, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | July 29, 2025 |
| Macleods Pharmaceuticals Limited | 3 | tablet | Generic drugs (ANDA) | October 16, 2024 |
| Major Pharmaceuticals | 3 | tablet, film coated | Generic drugs (ANDA) | November 3, 2025 |
| NorthStar RxLLC | 3 | tablet, film coated | Generic drugs (ANDA) | June 29, 2026 |
| Novadoz Pharmaceuticals LLC | 3 | tablet, film coated | Generic drugs (ANDA) | July 16, 2025 |
| Somerset Therapeutics, LLC | 3 | tablet, film coated | Generic drugs (ANDA) | February 21, 2026 |
| Umedica Laboratories USA Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | August 10, 2026 |
| XLCare Pharmaceuticals, Inc. | 3 | tablet | Generic drugs (ANDA) | September 30, 2025 |
| Zydus Lifesciences Limited | 3 | tablet | Generic drugs (ANDA) | July 8, 2025 |
| Zydus Pharmaceuticals USA Inc. | 3 | tablet | Generic drugs (ANDA) | July 8, 2025 |
| Coupler LLC | 1 | tablet, film coated | Generic drugs (ANDA) | December 16, 2025 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 81 | 78.6% |
| Tablet | 20 | 19.4% |
| Pellet | 2 | 1.9% |
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.