Data / Drug companies / Rabeprazole sodium
Rabeprazole sodium: 20 companies and 37 products in the FDA NDC directory
Rabeprazole sodium is listed in the FDA National Drug Code Directory by 20 companies, with 37 products in commercial distribution. 36 of the products (97.3%) 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 December 8, 2025.
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- Companies listing it
- 20
- Products
- 37
- Generic (ANDA) products
- 36 (97.3%)
- Application numbers
- 6
- Routes
- Oral
- Brand names
- Aciphex
- openFDA record search
- api.fda.gov
Companies that list rabeprazole sodium
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Advanced Rx of Tennessee, LLC | 4 | tablet, delayed release | Generic drugs (ANDA) | November 15, 2024 |
| Bryant Ranch Prepack | 4 | tablet, delayed release | Generic drugs (ANDA) | April 27, 2018 |
| Asclemed USA, Inc. | 3 | tablet, delayed release | Generic drugs (ANDA) | April 27, 2018 |
| Preferred Pharmaceuticals Inc. | 3 | tablet, delayed release | Generic drugs (ANDA) | December 8, 2025 |
| A-S Medication Solutions | 2 | tablet, delayed release | Generic drugs (ANDA) | April 27, 2018 |
| Bryant Ranch Prepack | 2 | tablet, delayed release | Generic drugs (ANDA) | April 27, 2018 |
| Direct_Rx | 2 | tablet, delayed release | Generic drugs (ANDA) | January 14, 2021 |
| Proficient Rx LP | 2 | tablet, delayed release | Generic drugs (ANDA) | November 8, 2013 |
| Proficient Rx LP | 2 | tablet, delayed release | Generic drugs (ANDA) | April 27, 2018 |
| Remedyrepack Inc. | 2 | tablet, delayed release | Generic drugs (ANDA) | September 1, 2021 |
| St. Mary's Medical Park Pharmacy | 2 | tablet, delayed release | Generic drugs (ANDA) | May 6, 2021 |
| Advagen Pharma Ltd | 1 | tablet, delayed release | Generic drugs (ANDA) | June 1, 2017 |
| Ascend Laboratories, LLC | 1 | tablet, delayed release | Generic drugs (ANDA) | April 27, 2018 |
| Aurobindo Pharma Limited | 1 | tablet, delayed release | Generic drugs (ANDA) | February 17, 2017 |
| Chartwell RX, LLC | 1 | tablet, delayed release | Generic drugs (ANDA) | November 8, 2013 |
| Golden State Medical Supply, Inc. | 1 | tablet, delayed release | Generic drugs (ANDA) | November 8, 2013 |
| Lannett Company, Inc. | 1 | tablet, delayed release | Generic drugs (ANDA) | November 8, 2013 |
| Phoenix RX LLC | 1 | tablet, delayed release | Generic drugs (ANDA) | April 27, 2018 |
| Torrent Pharmaceuticals Limited | 1 | tablet, delayed release | Generic drugs (ANDA) | November 8, 2013 |
| Waylis Therapeutics LLC | 1 | tablet, delayed release | New drug applications (NDA) | May 15, 2022 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, delayed release | 37 | 100% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 36 | 97.3% |
| New drug applications (NDA) | 1 | 2.7% |
Pharmacologic classes
| Class | Products |
|---|---|
| Proton Pump Inhibitor | 37 |
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.