PlainRecalls
FDA Drug Low Class III Terminated

Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Extended Release Tablets USP Allergy & Congestion, 20 Tablets, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ 08540, NDC 43598-823-14.

Reported: December 15, 2021 Initiated: November 12, 2021 #D-0269-2022

Product Description

Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Extended Release Tablets USP Allergy & Congestion, 20 Tablets, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ 08540, NDC 43598-823-14.

Reason for Recall

Failed dissolution specifications

Details

Units Affected
5016 cartons
Distribution
USA Nationwide.
Location
Princeton, NJ

Frequently Asked Questions

What product was recalled?
Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Extended Release Tablets USP Allergy & Congestion, 20 Tablets, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ 08540, NDC 43598-823-14.. Recalled by Dr. Reddy's Laboratories, Inc.. Units affected: 5016 cartons.
Why was this product recalled?
Failed dissolution specifications
Which agency issued this recall?
This recall was issued by the FDA Drug on December 15, 2021. Severity: Low. Recall number: D-0269-2022.