Ascend Laboratories recalls 30-count 5mg/40mg Amlodipine and Olmesartan Medoxomil tablets (NDC 67877-501-30) manufactured by Alkem Laboratories in India. The tablets may not dissolve properly, potentially affecting medication effectiveness.
Failed Dissolution Specifications: low dissolution results
Ascend Laboratories is recalling 30-count bottles of 5mg/40mg Amlodipine and Olmesartan Medoxomil tablets because they may not dissolve properly. This could lead to incorrect medication dosing if the tablets don't release their active ingredients as intended.
The tablets may not dissolve properly in the body, which could lead to incorrect medication dosing. This happens because the medication might not release its active ingredients at the right rate, potentially affecting how well it works for blood pressure or heart conditions.
Prescription medication users who received this specific 30-count bottle of Amlodipine and Olmesartan Medoxomil tablets from Ascend Laboratories. Patients taking blood pressure or heart conditions medication are most at risk if they use the tablets without proper dissolution.
Check for the 30-count bottle labeled 5mg/40mg Amlodipine and Olmesartan Medoxomil, manufactured by Alkem Laboratories in India, with NDC 67877-501-30. The lot number is 23121560, and it expires April 30, 2026.
Verify the product label matches the recalled items: 30-count bottle, 5mg/40mg Amlodipine and Olmesartan Medoxomil, NDC 67877-501-30, manufactured by Alkem Laboratories in India.
The recall is for potential issues with medication dissolution, but the product is safe to use if it's not the recalled batch. Always check the NDC number and lot number on the label.
The recall record does not specify a remedy, so contact your healthcare provider for guidance on whether to continue using the medication.
Check the label for NDC 67877-501-30, 30-count bottle, 5mg/40mg Amlodipine and Olmesartan Medoxomil, manufactured by Alkem Laboratories in India, with lot number 23121560.
We’ve drafted a message you can send Ascend Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0576-2025 — Ascend Laboratories Ascend Laboratories Hello, I own a Ascend Laboratories that is covered by recall D-0576-2025 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.
