Dr. Reddy's Ezetimibe and Simvastatin Tablets (10mg/80mg) with NDC codes 43598-745-30, 43598-745-90, and 43598-745-05 are recalled due to failed excipient specifications. This may affect medication safety.
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Dr. Reddy's Ezetimibe and Simvastatin Tablets (10 mg/80 mg) with specific NDC codes are recalled because the manufacturing process used an excipient that failed quality tests for conductivity. This could impact medication safety.
The tablets were manufactured using an excipient (a substance that helps the drug mix) that failed quality tests for conductivity. This could potentially affect the drug's performance or safety, though the exact risk is not clearly described in the recall notice.
People who have been prescribed these tablets by a healthcare provider and are using the recalled products. Those with high cholesterol or cardiovascular conditions may be at higher risk.
Check the product label for the NDC codes: 43598-745-30 (30 count), 43598-745-90 (90 count), or 43598-745-05 (500 count). These are prescription-only tablets.
Look for the NDC codes 43598-745-30, 43598-745-90, or 43598-745-05 on the tablet packaging.
The tablets were manufactured using an excipient that failed quality tests for conductivity, which could impact medication safety.
The recall notice does not specify a remedy, so contact your healthcare provider for advice.
The recall indicates a potential safety issue, but the exact risk is not clearly described in the notice.
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-0083-2022 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0083-2022 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.
