Dr. Reddy's recalls 20mg omeprazole capsules with foreign Divalproex Sodium tablets. Consumers should check NDC 82009-022-10 and lot C2403017 for affected products.
Presence of foreign tablets/capsules: presence of foreign Divalproex Sodium Extended-Release 250mg tablet in a bottle of omeprazole capsules.
Dr. Reddy's is recalling 20mg omeprazole capsules that contain foreign Divalproex Sodium tablets. This could cause harm if taken by mistake, as the foreign tablets are not intended for use.
The capsules contain foreign Divalproex Sodium Extended-Release tablets that are not meant to be taken with omeprazole. If someone takes the foreign tablets by mistake, it could cause harm due to the different medication.
People who have the specific 20mg omeprazole capsules with NDC 82009-022-10 and lot number C2403017. Those taking omeprazole for acid reflux or ulcers are most at risk if they accidentally consume the foreign tablets.
Check for the NDC code 82009-022-10 and lot number C2403017 on the product label. The product is a 1000-count bottle of 20mg omeprazole capsules, prescription-only.
Look for NDC 82009-022-10 and lot number C2403017 on the bottle.
The product contains foreign tablets that could cause harm if taken by mistake, so it is not safe to use as is.
Check for NDC 82009-022-10 and lot number C2403017 on the product label.
The recall does not specify a remedy, so contact Dr. Reddy's 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-0525-2025 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0525-2025 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.