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Dr. Reddy's Laboratories, Inc. recalls Fexofenadine HCl, 60 mg & Pseudoephedrine HCl 120 mg, Extended Release Tablets USP, Allergy and Congestion, 30 Tablets,

Recalled December 15, 2021 · FDA recall D-0275-2022 · Dr. Reddy's Laboratories

Hazard
Failed dissolution specifications · FDA Class III
Units
2,928 cartons
Sold at
USA Nationwide.

Description

Failed dissolution specifications

Product
Fexofenadine HCl, 60 mg & Pseudoephedrine HCl 120 mg, Extended Release Tablets USP, Allergy and Congestion, 30 Tablets, Distributed by: Dr. Reddy's Laboratories, Inc., Princeton, NJ, 08640, Made in India NDC Walmart Inc., Bentonville, AR 72716, Product of India, NDC 43598-823-31.
Manufacturer(s)
Dr. Reddy's Laboratories, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Dr. Reddy's Laboratories, Inc. recalls Fexofenadine HCl, 60 mg & Pseudoephedrine HCl 120 mg, Extended Release Tablets USP, Allergy and Congestion, 30 Tablets, | RecallWatchUSA