Dr. Reddy's Laboratories, Inc. recalls Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into c
Recalled January 26, 2022 · FDA recall D-0388-2022 · Dr. Reddy's Laboratories
Hazard
Subpotent drug · FDA Class III
Units
18336 cartons
Sold at
USA Nationwide
Description
Subpotent drug
Product
Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into cartons, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, Made in India, NDC 0363-164-3
Manufacturer(s)
Dr. Reddy's Laboratories, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →