Amneal Pharmaceuticals recalls 250mg Divalproex Sodium Extended-release Tablets due to failed dissolution specifications. This may affect medication effectiveness. Check NDC 65162-755-10 and lot numbers AR210704-09 for affected products.
Failed dissolution specifications
Amneal Pharmaceuticals is recalling 250mg Divalproex Sodium Extended-release Tablets because they failed dissolution specifications. This means the medication may not work as intended, potentially affecting treatment effectiveness.
The tablets failed dissolution specifications, meaning they may not release the medication properly in the body. This could lead to inconsistent drug levels and reduced effectiveness of the treatment. The issue is related to manufacturing quality control.
People who have the specific 250mg Divalproex Sodium Extended-release Tablets with NDC 65162-755-10 and lot numbers AR210704 through AR210709 are affected. Those using this medication for seizure disorders or other conditions are most at risk.
Check for NDC code 65162-755-10 and lot numbers AR210704 through AR210709 on the product packaging. These specific lot numbers were manufactured between April 2024 and the expiration date.
Look for NDC 65162-755-10 and lot numbers AR210704 through AR210709 on the tablet packaging.
The tablets failed dissolution specifications, which means they may not release medication properly and could be less effective.
Check the product details to see if it matches the recalled items. If it does, stop using it and contact your doctor for alternative treatment options.
The recall is due to potential reduced effectiveness, not immediate safety risks. However, using an ineffective medication could lead to treatment complications.
We’ve drafted a message you can send Amneal Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0426-2024 — Amneal Pharmaceuticals Amneal Pharmaceuticals Hello, I own a Amneal Pharmaceuticals that is covered by recall D-0426-2024 from Amneal Pharmaceuticals. 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.
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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.
