Data / Drug companies / Olmesartan medoxomil-hydrochlorothiazide
Olmesartan medoxomil-hydrochlorothiazide: 4 companies and 15 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Olmesartan medoxomil-hydrochlorothiazide is listed in the FDA National Drug Code Directory by 4 companies, with 15 products in commercial distribution. 3 of the products (20.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated, and the newest product started marketing on July 14, 2026.
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- Companies listing it
- 4
- Products
- 15
- Generic (ANDA) products
- 3 (20.0%)
- Application numbers
- 2
- Routes
- Oral
- Brand names
- Benicar HCT
- openFDA record search
- api.fda.gov
Companies that list olmesartan medoxomil-hydrochlorothiazide
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Cosette Pharmaceuticals, Inc. | 6 | tablet, film coated | New drug applications (NDA) | April 1, 2026 |
| AvKARE | 3 | tablet, film coated | New drug applications (NDA) | July 27, 2023 |
| AvKARE | 3 | tablet, film coated | New drug applications (NDA) | July 14, 2026 |
| Novadoz Pharmaceuticals LLC | 3 | tablet, film coated | Generic drugs (ANDA) | September 26, 2025 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 15 | 100% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| New drug applications (NDA) | 12 | 80% |
| Generic drugs (ANDA) | 3 | 20% |
Pharmacologic classes
| Class | Products |
|---|---|
| Angiotensin 2 Receptor Blocker | 15 |
| Thiazide Diuretic | 15 |
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.