Data / Drug companies / Benazepril hydrochloride and hydrochlorothiazide
Benazepril hydrochloride and hydrochlorothiazide: 7 companies and 21 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Benazepril hydrochloride and hydrochlorothiazide is listed in the FDA National Drug Code Directory by 7 companies, with 21 products in commercial distribution. 12 of the products (57.1%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; tablet, film coated, and the newest product started marketing on December 5, 2024.
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- Companies listing it
- 7
- Products
- 21
- Generic (ANDA) products
- 12 (57.1%)
- Application numbers
- 3
- Routes
- Oral
- Brand names
- Lotensin HCT
- openFDA record search
- api.fda.gov
Companies that list benazepril hydrochloride and hydrochlorothiazide
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Ani Pharmaceuticals, Inc. | 4 | tablet | Generic drugs (ANDA) | November 7, 2022 |
| Glenmark Pharmaceuticals Inc., USA | 4 | tablet, film coated | Generic drugs (ANDA) | March 17, 2015 |
| Sandoz Inc | 4 | tablet, film coated | Generic drugs (ANDA) | March 17, 2015 |
| Advagen Pharma Ltd | 3 | tablet | Authorized generics (NDA) | December 5, 2024 |
| Validus Pharmaceuticals LLC | 3 | tablet | New drug applications (NDA) | May 30, 1992 |
| Padagis US LLC | 2 | tablet | Authorized generics (NDA) | April 7, 2019 |
| Bryant Ranch Prepack | 1 | tablet | Authorized generics (NDA) | April 7, 2019 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 13 | 61.9% |
| Tablet, film coated | 8 | 38.1% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 12 | 57.1% |
| Authorized generics (NDA) | 6 | 28.6% |
| New drug applications (NDA) | 3 | 14.3% |
Pharmacologic classes
| Class | Products |
|---|---|
| Angiotensin Converting Enzyme Inhibitor | 21 |
| Thiazide Diuretic | 21 |
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.