Lupin Pharmaceuticals Inc. recalls Quinapril Tablets USP 5 mg, 90 count bottles, Lupin Pharmaceuticals, Inc., Baltimore, MD --- NDC 68180-556-09
Recalled April 12, 2017 · FDA recall D-0650-2017 · Lupin Pharmaceuticals
Hazard
Failed Impurities/Degradation Specifications; Impurity A · FDA Class III
Units
15,168 bottes
Sold at
Nationwide
Description
Failed Impurities/Degradation Specifications; Impurity A
Product
Quinapril Tablets USP 5 mg, 90 count bottles, Lupin Pharmaceuticals, Inc., Baltimore, MD --- NDC 68180-556-09
Manufacturer(s)
Lupin Pharmaceuticals Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →