Drug
Who makes amlodipine besylate and benazepril hydrochloride?
11 companies list amlodipine besylate and benazepril hydrochloride as a human prescription drug, including under the names Lotrel. Forms: capsule. Routes: oral.
Labellers from the openFDA NDC Directory. A labeller is the firm named on the label, not necessarily the site that made the product, and a listing is not an FDA approval. Data as of 24 Sept 2026. Methodology
Companies listing amlodipine besylate and benazepril hydrochloride
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| Lupin LimitedIndia | capsule | ANDAANDA078466 | 10 | 14 |
| Dr. Reddy's Laboratories LimitedIndia | capsule | ANDAANDA077183, ANDA090149 | 6 | 15 |
| International Medication Systems, Ltd.United States | capsule | ANDAANDA077183, ANDA078466 | 6 | 3 |
| Bryant Ranch PrepackUnited States | capsule | ANDAANDA078466 | 6 | 1 |
| BluePoint Laboratories Inc. | capsule | ANDAANDA078466 | 6 | 0 |
| RemedyRepack, IncUnited States | capsule | ANDAANDA077183, ANDA078466, ANDA090149 | 5 | 1 |
| Novartis Pharmaceuticals CorporationSwitzerland | capsule | NDANDA020364 | 4 | 20 |
| Amneal Pharmaceuticals NY LLC | capsule | ANDAANDA077215 | 4 | 0 |
| Northwind Health Company, LLCUnited States | capsule | ANDAANDA077183 | 2 | 1 |
| PD-Rx Pharmaceuticals Inc.United States | capsule | ANDAANDA078466 | 2 | 1 |
| Preferred Pharmaceuticals Inc.United States | capsule | ANDAANDA078466 | 1 | 1 |
Enquiry
Common questions
- Who makes amlodipine besylate and benazepril hydrochloride?
- 11 companies list amlodipine besylate and benazepril hydrochloride as a human prescription drug in the openFDA NDC Directory, led by Lupin Limited, Dr. Reddy's Laboratories Limited, International Medication Systems, Ltd., Bryant Ranch Prepack, BluePoint Laboratories Inc.. Each is the labeller, the firm named on the label; the product may be made at a site registered to another company.
- Is there a generic Lotrel?
- 10 companies list amlodipine besylate and benazepril hydrochloride under an abbreviated new drug application (ANDA), the application type used for generics, and 1 under an NDA or BLA. Listing status is from the NDC Directory; it is not a statement of availability.