Data / Drug companies / Bisoprolol fumarate and hydrochlorothiazide
Bisoprolol fumarate and hydrochlorothiazide: 12 companies and 42 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Bisoprolol fumarate and hydrochlorothiazide is listed in the FDA National Drug Code Directory by 12 companies, with 42 products in commercial distribution. 38 of the products (90.5%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; tablet, and the newest product started marketing on January 21, 2026.
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- Companies listing it
- 12
- Products
- 42
- Generic (ANDA) products
- 38 (90.5%)
- Application numbers
- 8
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list bisoprolol fumarate and hydrochlorothiazide
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| A-S Medication Solutions | 6 | tablet, film coated; tablet | Generic drugs (ANDA) | January 26, 2022 |
| Bryant Ranch Prepack | 6 | tablet, film coated; tablet | Generic drugs (ANDA) | January 26, 2022 |
| Ani Pharmaceuticals, Inc. | 3 | tablet | Generic drugs (ANDA) | November 4, 2021 |
| Aurobindo Pharma Limited | 3 | tablet, film coated | Generic drugs (ANDA) | January 21, 2026 |
| Edenbridge Pharmaceuticals LLC. | 3 | tablet, film coated | Generic drugs (ANDA) | April 30, 2019 |
| Glenmark Pharmaceuticals Inc., USA | 3 | tablet, film coated | Generic drugs (ANDA) | January 26, 2022 |
| Marlex Pharmaceuticals, Inc. | 3 | tablet | Generic drugs (ANDA) | May 1, 2022 |
| Mylan Pharmaceuticals Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | February 22, 2021 |
| Teva Pharmaceuticals USA, Inc. | 3 | tablet, film coated | Authorized generics (NDA) | August 7, 2019 |
| Unichem Pharmaceuticals (USA), Inc. | 3 | tablet | Generic drugs (ANDA) | October 12, 2010 |
| Viona Pharmaceuticals Inc | 3 | tablet, film coated | Generic drugs (ANDA) | March 1, 2023 |
| Zydus Lifesciences Limited | 3 | tablet, film coated | Generic drugs (ANDA) | March 1, 2023 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 30 | 71.4% |
| Tablet | 12 | 28.6% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 38 | 90.5% |
| Authorized generics (NDA) | 4 | 9.5% |
Pharmacologic classes
| Class | Products |
|---|---|
| Thiazide Diuretic | 42 |
| beta-Adrenergic Blocker | 42 |
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.