Data / Drug companies / Dipeptidyl Peptidase 4 Inhibitor
Dipeptidyl Peptidase 4 Inhibitor drugs: 16 drugs from 21 companies in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Dipeptidyl Peptidase 4 Inhibitor is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 127 products in this class from 21 companies, covering 16 drugs by generic name. The main marketing category is new drug applications (NDA), and the newest product started marketing on July 24, 2026.
The request: Get every company that lists a Dipeptidyl Peptidase 4 Inhibitor drug in the FDA NDC directory, with headquarters, website and size. $10 of work on sign-up, no card.
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.
- 21Companies
- 127Products
- 16Drugs by generic name
Drugs in the Dipeptidyl Peptidase 4 Inhibitor class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Sitagliptin and metformin hydrochloride | 37 | 8 |
| Sitagliptin | 32 | 8 |
| Alogliptin | 10 | 5 |
| Saxagliptin | 6 | 3 |
| Alogliptin and metformin hydrochloride | 5 | 3 |
| Linagliptin | 3 | 3 |
| Linagliptin and metformin hydrochloride | 8 | 2 |
| Alogliptin and pioglitazone | 4 | 1 |
| Alogliptin benzoate and pioglitazone hydrochloride | 4 | 1 |
| Empagliflozin, linagliptin, metformin hydrochloride | 4 | 1 |
| Saxagliptin and metformin | 3 | 1 |
| Saxagliptin and metformin hydrochloride | 3 | 1 |
| Sitagliptin phosphate | 3 | 1 |
| Empagliflozin and linagliptin | 2 | 1 |
| Ertugliflozin and sitagliptin | 2 | 1 |
| Sitagliptin hydrochloride oral | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Zydus Lifesciences Limited | 16 | tablet; tablet, film coated, extended release | Authorized generics (NDA) | October 31, 2024 |
| Zydus Pharmaceuticals USA Inc. | 16 | tablet, film coated, extended release; tablet | New drug applications (NDA) | October 31, 2024 |
| A-S Medication Solutions | 12 | tablet, film coated; tablet, film coated, extended release | New drug applications (NDA) | April 8, 2016 |
| Boehringer Ingelheim Pharmaceuticals, Inc. | 12 | tablet, film coated; tablet, extended release | New drug applications (NDA) | April 23, 2020 |
| Merck Sharp & Dohme LLC | 10 | tablet, film coated; tablet, film coated, extended release | New drug applications (NDA) | December 19, 2017 |
| Padagis Israel Pharmaceuticals Ltd | 9 | tablet, film coated | Authorized generics (NDA) | April 8, 2016 |
| Takeda Pharmaceuticals America, Inc. | 9 | tablet, film coated | New drug applications (NDA) | January 25, 2013 |
| Apotex Corp. | 5 | tablet, film coated | Generic drugs (ANDA) | May 28, 2026 |
| Golden State Medical Supply, Inc. | 5 | tablet, film coated | Generic drugs (ANDA) | April 30, 2026 |
| Mylan Pharmaceuticals Inc. | 5 | tablet, film coated, extended release; tablet, film coated | Generic drugs (ANDA) | August 8, 2023 |
| Sandoz Inc | 5 | tablet, film coated | Generic drugs (ANDA) | May 28, 2026 |
| Cardinal Health 107, LLC | 3 | tablet, film coated | New drug applications (NDA) | May 9, 2011 |
| Dr. Reddy's Laboratories Inc. | 3 | tablet, film coated, extended release | Generic drugs (ANDA) | August 9, 2023 |
| Novadoz Pharmaceuticals LLC | 3 | tablet, film coated | Generic drugs (ANDA) | November 3, 2025 |
| Par Health USA, LLC | 3 | tablet, film coated, extended release | Generic drugs (ANDA) | July 24, 2026 |
| Teva Pharmaceuticals, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | May 28, 2026 |
| Aphena Pharma Solutions - Tennessee, LLC | 2 | tablet, film coated | Authorized generics (NDA) | April 8, 2016 |
| Aurobindo Pharma Limited | 2 | tablet, film coated | Generic drugs (ANDA) | July 31, 2023 |
| Glenmark Pharmaceuticals Inc., USA | 2 | tablet, film coated | Generic drugs (ANDA) | July 31, 2023 |
| Azurity Pharmaceuticals, Inc. | 1 | solution | New drug applications (NDA) | April 1, 2025 |
| Bryant Ranch Prepack | 1 | tablet, film coated | Authorized generics (NDA) | April 8, 2016 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 83 | 65.4% |
| Tablet, film coated, extended release | 27 | 21.3% |
| Tablet | 12 | 9.4% |
| Tablet, extended release | 4 | 3.1% |
| Solution | 1 | 0.8% |
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.