Data / Drug companies / Nebivolol hydrochloride
Nebivolol hydrochloride: 5 companies and 20 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Nebivolol hydrochloride is listed in the FDA National Drug Code Directory by 5 companies, with 20 products in commercial distribution. 16 of the products (80.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, and the newest product started marketing on July 10, 2024.
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- Companies listing it
- 5
- Products
- 20
- Generic (ANDA) products
- 16 (80.0%)
- Application numbers
- 4
- Routes
- Oral
- Brand names
- Nebivolol, Bystolic
- openFDA record search
- api.fda.gov
Companies that list nebivolol hydrochloride
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Allergan, Inc. | 4 | tablet | New drug applications (NDA) | January 22, 2008 |
| Apnar Pharma LP | 4 | tablet | Generic drugs (ANDA) | May 13, 2024 |
| AvKARE | 4 | tablet | Generic drugs (ANDA) | July 10, 2024 |
| Glenmark Pharmaceuticals Inc., USA | 4 | tablet | Generic drugs (ANDA) | May 25, 2017 |
| Unichem Pharmaceuticals (USA), Inc. | 4 | tablet | Generic drugs (ANDA) | April 4, 2022 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 20 | 100% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 16 | 80% |
| New drug applications (NDA) | 4 | 20% |
Pharmacologic classes
| Class | Products |
|---|---|
| beta-Adrenergic Blocker | 20 |
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.