Data / Drug companies / Amlodipine and benazepril hydrochloride
Amlodipine and benazepril hydrochloride: 14 companies and 41 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Amlodipine and benazepril hydrochloride is listed in the FDA National Drug Code Directory by 14 companies, with 41 products in commercial distribution. 41 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 July 24, 2026.
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- Companies listing it
- 14
- Products
- 41
- Generic (ANDA) products
- 41 (100.0%)
- Application numbers
- 2
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list amlodipine and benazepril hydrochloride
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 | 7 | capsule | Generic drugs (ANDA) | September 5, 2012 |
| Aurobindo Pharma Limited | 6 | capsule | Generic drugs (ANDA) | September 5, 2012 |
| Golden State Medical Supply, Inc. | 6 | capsule | Generic drugs (ANDA) | December 30, 2013 |
| Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc. | 6 | capsule | Generic drugs (ANDA) | July 24, 2026 |
| Rising Pharma Holdings, Inc. | 6 | capsule | Generic drugs (ANDA) | September 5, 2012 |
| PD-Rx Pharmaceuticals, Inc. | 2 | capsule | Generic drugs (ANDA) | September 5, 2012 |
| Bryant Ranch Prepack | 1 | capsule | Generic drugs (ANDA) | September 5, 2012 |
| Bryant Ranch Prepack | 1 | capsule | Generic drugs (ANDA) | September 5, 2012 |
| Bryant Ranch Prepack | 1 | capsule | Generic drugs (ANDA) | September 5, 2012 |
| Direct_Rx | 1 | capsule | Generic drugs (ANDA) | August 10, 2021 |
| Northwind Health Company, LLC | 1 | capsule | Generic drugs (ANDA) | October 20, 2022 |
| Preferred Pharmaceuticals Inc. | 1 | capsule | Generic drugs (ANDA) | June 2, 2023 |
| Proficient Rx LP | 1 | capsule | Generic drugs (ANDA) | September 5, 2012 |
| Remedyrepack Inc. | 1 | capsule | Generic drugs (ANDA) | March 1, 2019 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule | 41 | 100% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 41 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Angiotensin Converting Enzyme Inhibitor | 41 |
| Calcium Channel Blocker | 41 |
| Dihydropyridine Calcium Channel Blocker | 41 |
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.