Dr. Reddy's recalls 20-tablet allergy/congestion medication due to failed dissolution specifications. Consumers should check NDC 43598-823-14 and lot numbers for affected products.
Failed dissolution specifications
Dr. Reddy's is recalling fexofenadine and pseudoephedrine extended-release tablets because they failed dissolution specifications. This means the medication may not work as intended, potentially causing ineffective allergy and congestion treatment.
The medication failed dissolution specifications, meaning it may not release the active ingredients properly in the body. This could lead to the medication not working as intended for allergy and congestion relief.
People who purchased the 20-tablet allergy and congestion medication with NDC 43598-823-14 and lot number AC2103329F are affected. Those with allergies or congestion symptoms may be at higher risk of ineffective treatment.
Check for the NDC code 43598-823-14 and lot number AC2103329F on the product packaging. The product was distributed by Dr. Reddy's Laboratories, Inc. in Princeton, NJ.
Look for NDC 43598-823-14 and lot number AC2103329F on the packaging to confirm if the product is affected.
The recall is due to failed dissolution specifications, which may mean the medication doesn't work as intended. It is not recommended to use the affected product.
Check the NDC code 43598-823-14 and lot number AC2103329F on the product packaging.
The recall does not specify a remedy, so contact Dr. Reddy's Laboratories, Inc. for guidance.
We’ve drafted a message you can send Dr. Reddy's to request your refund or repair — edit it as you like.
Subject: Recall D-0269-2022 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0269-2022 from Dr. Reddy's. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.