Data / Drug companies / Pantoprazole
Pantoprazole: 25 companies and 51 products in the FDA NDC directory
Pantoprazole is listed in the FDA National Drug Code Directory by 25 companies, with 51 products in commercial distribution. 51 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, delayed release, and the newest product started marketing on August 26, 2026.
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- Companies listing it
- 25
- Products
- 51
- Generic (ANDA) products
- 51 (100.0%)
- Application numbers
- 3
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list pantoprazole
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| NuCare Pharmaceuticals,Inc. | 6 | tablet, delayed release | Generic drugs (ANDA) | December 15, 2023 |
| Asclemed USA, Inc. | 4 | tablet, delayed release | Generic drugs (ANDA) | May 1, 2022 |
| Proficient Rx LP | 4 | tablet, delayed release | Generic drugs (ANDA) | June 20, 2016 |
| Bryant Ranch Prepack | 3 | tablet, delayed release | Generic drugs (ANDA) | June 20, 2016 |
| A-S Medication Solutions | 2 | tablet, delayed release | Generic drugs (ANDA) | September 10, 2014 |
| Amneal Pharmaceuticals LLC | 2 | tablet, delayed release | Generic drugs (ANDA) | June 20, 2016 |
| Aphena Pharma Solutions - Tennessee, LLC | 2 | tablet, delayed release | Generic drugs (ANDA) | May 1, 2022 |
| Camber Pharmaceuticals, Inc. | 2 | tablet, delayed release | Generic drugs (ANDA) | September 10, 2014 |
| Dr. Reddy's Laboratories Limited | 2 | tablet, delayed release | Generic drugs (ANDA) | January 19, 2011 |
| Hawaii Repack, Inc. | 2 | tablet, delayed release | Generic drugs (ANDA) | September 10, 2014 |
| NorthStar RxLLC | 2 | tablet, delayed release | Generic drugs (ANDA) | December 15, 2023 |
| Phoenix RX LLC | 2 | tablet, delayed release | Generic drugs (ANDA) | June 20, 2016 |
| Preferred Pharmaceuticals Inc. | 2 | tablet, delayed release | Generic drugs (ANDA) | May 1, 2024 |
| Quallent Pharmaceuticals Health LLC | 2 | tablet, delayed release | Generic drugs (ANDA) | June 6, 2022 |
| Sportpharm LLC | 2 | tablet, delayed release | Generic drugs (ANDA) | September 10, 2014 |
| St. Mary's Medical Park Pharmacy | 2 | tablet, delayed release | Generic drugs (ANDA) | October 31, 2022 |
| XLCare Pharmaceuticals, Inc. | 2 | tablet, delayed release | Generic drugs (ANDA) | May 1, 2022 |
| Advanced Rx of Tennessee, LLC | 1 | tablet, delayed release | Generic drugs (ANDA) | October 15, 2025 |
| AvPAK | 1 | tablet, delayed release | Generic drugs (ANDA) | August 26, 2026 |
| Coupler LLC | 1 | tablet, delayed release | Generic drugs (ANDA) | June 19, 2026 |
| Direct_Rx | 1 | tablet, delayed release | Generic drugs (ANDA) | June 12, 2020 |
| Northwind Health Company, LLC | 1 | tablet, delayed release | Generic drugs (ANDA) | July 9, 2021 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, delayed release | Generic drugs (ANDA) | September 10, 2014 |
| QPharma, Inc. | 1 | tablet, delayed release | Generic drugs (ANDA) | September 10, 2014 |
| Redpharm Drug | 1 | tablet, delayed release | Generic drugs (ANDA) | January 19, 2011 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, delayed release | 51 | 100% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 51 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Proton Pump Inhibitor | 51 |
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.