Ascend Laboratories recalls 10mg/20mg Amlodipine and Olmesartan Medoxomil tablets (NDC 67877-500-30) due to failed dissolution specs causing low drug content. Rx only, manufactured in India, distributed in US.
Failed Dissolution Specifications; Olmesartan Medoxomil content below specifications
Ascend Laboratories is recalling certain blood pressure medication tablets because they contain less active ingredient than labeled. This could lead to ineffective treatment if taken without proper dosage. The recall applies to prescription-only tablets sold in the US.
The tablets failed to dissolve properly in the body, resulting in lower than expected levels of the active medication. This means the treatment might not work as intended, potentially leading to uncontrolled blood pressure. However, the risk is not immediate or life-threatening.
Prescription patients who received these specific tablets from Ascend Laboratories in the US. Those with uncontrolled hypertension may be at slightly higher risk if the medication isn't working properly.
Check for the product name 'Amlodipine and Olmesartan Medoxomil Tablets, 10 mg/20 mg, 30 Tablets per bottle' on the label. Look for NDC code 67877-500-30 and lot number 25121311 with expiration 3/31/2028.
Look for the NDC code 67877-500-30 and lot number 25121311 on the bottle.
The tablets contain less active ingredient than labeled, which could lead to ineffective treatment. However, the risk is not immediate or life-threatening.
Check for the NDC code 67877-500-30 and lot number 25121311 on the bottle label.
The recall record does not specify a remedy, so contact your doctor or pharmacist for guidance.
We’ve drafted a message you can send Ascend Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0712-2026 — Ascend Laboratories Ascend Laboratories Hello, I own a Ascend Laboratories that is covered by recall D-0712-2026 from Ascend Laboratories. 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.
