Drug
Who makes lisinopril and hydrochlorothiazide tablets?
11 companies list lisinopril and hydrochlorothiazide tablets as a human prescription drug. Forms: tablet. 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 lisinopril and hydrochlorothiazide tablets
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| International Medication Systems, Ltd.United States | tablet | ANDAANDA076230, ANDA204058 | 7 | 3 |
| Bryant Ranch PrepackUnited States | tablet | ANDAANDA076230, ANDA204058 | 5 | 1 |
| NuCare Pharmaceuticals,Inc.United States | tablet | ANDAANDA076230, ANDA204058 | 4 | 1 |
| Aphena Pharma Solutions - Tennessee, LLC | tablet | ANDAANDA076230, ANDA204058 | 4 | 0 |
| CIPLA PHARMACEUTICALS LIMITEDIndia | tablet | ANDAANDA204058 | 3 | 7 |
| Preferred Pharmaceuticals Inc.United States | tablet | ANDAANDA076230 | 3 | 1 |
| Exelan Pharmaceuticals, Inc. | tablet | ANDAANDA204058 | 3 | 0 |
| Solco healthcare U.S., LLC | tablet | ANDAANDA076230 | 3 | 0 |
| Proficient Rx LPUnited States | tablet | ANDAANDA076230 | 2 | 1 |
| RemedyRepack, IncUnited States | tablet | ANDAANDA076230 | 2 | 1 |
| St. Mary's Medical Park PharmacyUnited States | tablet | ANDAANDA076230 | 2 | 1 |
Enquiry
Common questions
- Who makes lisinopril and hydrochlorothiazide tablets?
- 11 companies list lisinopril and hydrochlorothiazide tablets as a human prescription drug in the openFDA NDC Directory, led by International Medication Systems, Ltd., Bryant Ranch Prepack, NuCare Pharmaceuticals,Inc., Aphena Pharma Solutions - Tennessee, LLC, CIPLA PHARMACEUTICALS LIMITED. 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 lisinopril and hydrochlorothiazide tablets?
- 11 companies list lisinopril and hydrochlorothiazide tablets under an abbreviated new drug application (ANDA), the application type used for generics. Listing status is from the NDC Directory; it is not a statement of availability.