Quick answers
- What is Lisinopril/HCTZ?
- Lisinopril/HCTZ is a brand name of Lisinopril and hydrochlorothiazide, a prescription medicine. The FDA NDC Directory lists 1 Lisinopril/HCTZ product in 1 strength and form.
- Who makes Lisinopril/HCTZ?
- Prinston Inc holds the FDA application for Lisinopril/HCTZ (ANDA076230, approved July 1, 2002).
- Is there a generic or store brand of Lisinopril/HCTZ?
- Yes. The FDA NDC Directory lists 33 other products with the same active ingredients, strength and form as a Lisinopril/HCTZ product, 32 of them generic. Ask your pharmacist whether one is right for you.
- Has Lisinopril/HCTZ been recalled?
- No recall linked to Lisinopril/HCTZ products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Lisinopril/HCTZ is
Each Lisinopril/HCTZ product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Lisinopril and hydrochlorothiazide · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| hydrochlorothiazide 12.5 mg · lisinopril 20 mg tablet (oral) | Lisinopril/HCTZ | 33 products, 20 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Lisinopril and hydrochlorothiazide →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA076230 | Prinston Inc | July 1, 2002 | 1 |
Companies that list Lisinopril/HCTZ
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Lisinopril/HCTZ products.
- Direct_Rx1 product
Recalls
No recall linked to Lisinopril/HCTZ products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.