Qualitest Pharmaceuticals recalls AMLODIPINE BESYLATE TABLETS USP, 10 mg*, 1000 count bottles (NDC 0603-2110-32), Rx only, Manufactured for: QUALITEST PH
Recalled March 11, 2015 · FDA recall D-0397-2015 · Qualitest Pharmaceuticals
Hazard
Failed tablet specifications: One lot was found to contain oversized tablets. · FDA Class II
Units
2808 bottles
Sold at
Nationwide
Description
Failed tablet specifications: One lot was found to contain oversized tablets.
Product
AMLODIPINE BESYLATE TABLETS USP, 10 mg*, 1000 count bottles (NDC 0603-2110-32), Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811
Manufacturer(s)
Qualitest Pharmaceuticals
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →