Drug
Who makes fosinopril sodium and hydrochlorothiazide?
2 companies list fosinopril sodium and hydrochlorothiazide 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 fosinopril sodium and hydrochlorothiazide
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| CIPLA PHARMACEUTICALS LIMITEDIndia | tablet | ANDAANDA090228 | 2 | 7 |
| Aurobindo Pharma LimitedIndia | tablet | ANDAANDA079245 | 1 | 6 |
Enquiry
Common questions
- Who makes fosinopril sodium and hydrochlorothiazide?
- 2 companies list fosinopril sodium and hydrochlorothiazide as a human prescription drug in the openFDA NDC Directory, led by CIPLA PHARMACEUTICALS LIMITED, Aurobindo Pharma 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 fosinopril sodium and hydrochlorothiazide?
- 2 companies list fosinopril sodium 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.