Glenmark Pharmaceuticals recalls 2.5mg/6.25mg Bisoprolol Fumarate and Hydrochlorothiazide tablets due to traces of ezetimibe found in some batches. Check NDC numbers for affected lots.
Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibe
Glenmark Pharmaceuticals is recalling certain Bisoprolol Fumarate and Hydrochlorothiazide tablets because testing found traces of ezetimibe. This cross-contamination could potentially lead to unintended medication interactions if taken.
Testing of reserve samples showed traces of ezetimibe, a cholesterol medication, in some batches of these tablets. This cross-contamination could cause unintended medication interactions if the tablets are taken without proper medical supervision.
People who have the specific 30-count, 100-count, or 500-count bottles of these tablets with the listed NDC numbers and expiration dates are affected. Those taking these medications for blood pressure or heart conditions are most at risk.
Check for NDC numbers: 68462-878-30 (30-count), 68462-878-01 (100-count), or 68462-878-05 (500-count). The affected lots have specific expiration dates and manufacturing dates listed in the recall notice.
Verify the NDC number on your bottle to see if it matches the recalled lots (68462-878-30, 68462-878-01, or 68462-878-05).
Testing of reserve samples showed traces of ezetimibe in some batches of these tablets, which could cause unintended medication interactions.
The recall notice does not specify a remedy; check the NDC number to confirm if your medication is affected and contact your doctor for advice.
Yes, the recalled lots have specific expiration dates: November 2025 for some and May 2026 for others.
We’ve drafted a message you can send Glenmark Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0199-2026 — Glenmark Pharmaceuticals Glenmark Pharmaceuticals Hello, I own a Glenmark Pharmaceuticals that is covered by recall D-0199-2026 from Glenmark 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.
