Drug
Who makes spironolactone and hydrochlorothiazide?
7 companies list spironolactone and hydrochlorothiazide as a human prescription drug. 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 spironolactone and hydrochlorothiazide
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| Bryant Ranch PrepackUnited States | tablet | ANDAANDA089534 | 6 | 1 |
| Sun Pharmaceutical Industries LimitedIndia | tablet | ANDAANDA089534 | 1 | 13 |
| Safecor Health, LLCUnited States | tablet | ANDAANDA086513 | 1 | 3 |
| Advagen Pharma Limited | tablet | ANDAANDA220884 | 1 | 0 |
| Mylan Institutional Inc. | tablet | ANDAANDA086513 | 1 | 0 |
| Mylan Pharmaceuticals, Inc. | tablet | ANDAANDA086513 | 1 | 0 |
| Prasco Laboratories | tablet, film coated | NDA AUTHORIZED GENERICNDA012616 | 1 | 0 |
Enquiry
Common questions
- Who makes spironolactone and hydrochlorothiazide?
- 7 companies list spironolactone and hydrochlorothiazide as a human prescription drug in the openFDA NDC Directory, led by Bryant Ranch Prepack, Sun Pharmaceutical Industries Limited, Safecor Health, LLC, Advagen Pharma Limited, Mylan Institutional 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 spironolactone and hydrochlorothiazide?
- 6 companies list spironolactone and hydrochlorothiazide 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.