Drug
Who makes irbesartan and hydrochlorothiazide?
11 companies list irbesartan and hydrochlorothiazide as a human prescription drug, including under the names Avalide. Forms: tablet; tablet, film coated. 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 irbesartan and hydrochlorothiazide
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| Alembic Pharmaceuticals LimitedIndia | tablet; tablet, film coated | ANDAANDA091370 | 6 | 7 |
| Bryant Ranch PrepackUnited States | tablet; tablet, film coated | ANDAANDA077369, ANDA090351, ANDA202414 | 6 | 1 |
| Aurobindo Pharma LimitedIndia | tablet, film coated | ANDAANDA203630 | 3 | 6 |
| Proficient Rx LPUnited States | tablet; tablet, film coated | ANDAANDA077369, ANDA202414, ANDA203072 | 3 | 1 |
| Teva Pharmaceutical Industries Ltd.Canada | tablet, film coated | ANDAANDA077369 | 2 | 6 |
| Macleods Pharmaceuticals LimitedIndia | tablet, film coated | ANDAANDA202414 | 2 | 5 |
| Unichem Laboratories Limited, IndiaIndia | tablet, film coated | ANDAANDA207018 | 2 | 5 |
| Hikma Pharmaceuticals USA Inc.United States | tablet | ANDAANDA090351 | 2 | 4 |
| Solco healthcare U.S., LLC | tablet | ANDAANDA203072 | 2 | 0 |
| sanofi-aventis U.S. LLC | tablet, film coated | NDANDA020758 | 2 | 0 |
| RemedyRepack, IncUnited States | tablet | ANDAANDA203072 | 1 | 1 |
Enquiry
Common questions
- Who makes irbesartan and hydrochlorothiazide?
- 11 companies list irbesartan and hydrochlorothiazide as a human prescription drug in the openFDA NDC Directory, led by Alembic Pharmaceuticals Limited, Bryant Ranch Prepack, Aurobindo Pharma Limited, Proficient Rx LP, Teva Pharmaceutical Industries Ltd.. 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 Avalide?
- 10 companies list irbesartan and hydrochlorothiazide 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.