Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg recall: Failed Dissolution
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.
Why was Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg recalled?
Failed dissolution specifications
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: AC2103329F, Exp 1/2023
- Product
- 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.
- Recalling firm
- Dr. Reddy's Laboratories, Inc.
- Quantity
- 5016 cartons
- Distribution
- USA Nationwide.
- Recall date
- December 15, 2021
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)