Dr. Reddy's Laboratories, Inc. recalls Dr. Reddys, Fexofenadine HCl 60 mg & Pseudoephedrine HCl 120 mg Extended-Release Tablets USP, a) 10 tablets per box, UPC
Recalled January 26, 2022 · FDA recall D-0382-2022 · Dr. Reddy's Laboratories
Hazard
Failed Dissolution Specifications · FDA Class III
Units
9,912 boxes
Sold at
Nationwide in the USA
Description
Failed Dissolution Specifications
Product
Dr. Reddys, Fexofenadine HCl 60 mg & Pseudoephedrine HCl 120 mg Extended-Release Tablets USP, a) 10 tablets per box, UPC 343598823355, b) 20 tablets per box, UPC 343598823140, c) 30 tablets per box, UPC 343598823317, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ 08540, Made in India.
Manufacturer(s)
Dr. Reddy's Laboratories, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →