Class III ยท Low risk
Vaseretic (enalapril maleate/hydrochlorothiazide)
Labeling: Incorrect or Missing Package Insert: Product is packaged with the incorrect version of the package outset
National Drug Code
Is NDC 0187-0146-01 recalled?
Vaseretic · 100 TABLET in 1 BOTTLE (0187-0146-01)
Yes — this exact package was recalled
1 FDA recall names the code 0187-0146-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- enalapril maleate and hydrochlorothiazide
- Strength
- ENALAPRIL MALEATE 10 mg/1; HYDROCHLOROTHIAZIDE 25 mg/1
- Form
- Tablet · Oral
- Labeler
- Bausch Health US, LLC
- Type
- Human Prescription Drug
- Product code
- 0187-0146
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
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