(The Hill) – Lupin Pharmaceuticals Inc. recalls four lots of its blood pressure medication, Quinapril Tablets, because of an impurity known as Nitrosamines being found in recent testing of the product, according to the Food and Drug Administration (FDA).
The FDA stated that no illness related to the medication has yet been reported and that the marketing of the Quinapril Tablets ended in September. Quinapril is an angiotensin-converting enzyme (ACE) inhibitor used to treat hypertension and lower blood pressure.
The tablets were contaminated by a substance known as Nitrosamines, which the FDA reports is commonly found in food and water.
Christmas Events This Weekend in the Lakes Region
Drought Levels Steady in Lakes Region
Nixa to Host Mayor’s Tree Lighting Ceremony and Community Cocoa Night on Dec. 5
Stone County Authorities Ask for Help in Locating Missing Teen
Green Forest Woman Faces Missouri Drug Charges