Data / Drug companies / Balsalazide disodium
Balsalazide disodium: 9 companies and 9 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Balsalazide disodium is listed in the FDA National Drug Code Directory by 9 companies, with 9 products in commercial distribution. 9 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule, and the newest product started marketing on June 30, 2025.
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- Companies listing it
- 9
- Products
- 9
- Generic (ANDA) products
- 9 (100.0%)
- Application numbers
- 4
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list balsalazide disodium
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Apotex Corp. | 1 | capsule | Generic drugs (ANDA) | December 28, 2007 |
| AvPAK | 1 | capsule | Generic drugs (ANDA) | November 6, 2014 |
| Bryant Ranch Prepack | 1 | capsule | Generic drugs (ANDA) | December 28, 2007 |
| Carnegie Pharmaceuticals LLC | 1 | capsule | Generic drugs (ANDA) | June 30, 2025 |
| Golden State Medical Supply, Inc. | 1 | capsule | Generic drugs (ANDA) | December 28, 2007 |
| Hikma Pharmaceuticals USA Inc. | 1 | capsule | Generic drugs (ANDA) | December 28, 2007 |
| PD-Rx Pharmaceuticals, Inc. | 1 | capsule | Generic drugs (ANDA) | December 28, 2007 |
| Zydus Lifesciences Limited | 1 | capsule | Generic drugs (ANDA) | August 25, 2023 |
| Zydus Pharmaceuticals USA Inc. | 1 | capsule | Generic drugs (ANDA) | August 25, 2023 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule | 9 | 100% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 9 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Aminosalicylate | 9 |
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.