Quick answers
- What is Vaseretic?
- Vaseretic is a brand name of Enalapril maleate and hydrochlorothiazide, a prescription medicine. The FDA NDC Directory lists 1 Vaseretic product in 1 strength and form.
- Who makes Vaseretic?
- Bausch holds the FDA application for Vaseretic (NDA019221, approved October 31, 1986).
- Is there a generic or store brand of Vaseretic?
- Yes. The FDA NDC Directory lists 2 other products with the same active ingredients, strength and form as a Vaseretic product, 2 of them generic. Ask your pharmacist whether one is right for you.
- Has Vaseretic been recalled?
- FDA enforcement reports list 1 recall of Vaseretic products; the newest started May 21, 2014. A recall usually concerns specific lots, not every product.
What Vaseretic is
Each Vaseretic 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.
Enalapril maleate and hydrochlorothiazide · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| enalapril maleate 10 mg · hydrochlorothiazide 25 mg tablet (oral) | Vaseretic | 2 products, 2 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Enalapril maleate and hydrochlorothiazide →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA019221 | Bausch | October 31, 1986 | 1 |
Companies that list Vaseretic
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Vaseretic products.
- Bausch Health US, LLC1 product
Recalls
From FDA enforcement reports, matched by the product’s NDC code or label. A recall usually covers specific lots: check the lot number on your package and ask your pharmacist. Do not stop a medicine on your own.
-
May 21, 2014 · Class III · Terminated · D-0018-2015
Labeling: Incorrect or Missing Package Insert: Product is packaged with the incorrect version of the package outset
Vaseretic (enalapril maleate/hydrochlorothiazide) 10/25 mg Tablets, NDC 0187-0146-01, 100 ct. bottles manufactured at Valeant Pharmaceuticals International, Inc., Steinbach, MD R5G 1Z7 Canada — Valeant Pharmaceuticals North America LLC
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.