Glenmark Pharmaceuticals recalls 50mg Lacosamide tablets due to manufacturing deviations. Affected products have specific NDC and lot numbers. Consumers should contact the company for details.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 50mg Lacosamide tablets that were manufactured with CGMP deviations. This recall affects prescription-only bottles sold in the U.S. with specific lot numbers and expiration dates.
CGMP deviations refer to manufacturing process issues that could affect product safety and quality. These deviations may lead to potential product failure or harm if the tablets are used as intended.
Prescription patients who received the recalled Lacosamide tablets with NDC 68462-678-60 and lot number 17240221. Those who have the tablets with an expiration date of January 26, 2027, are most at risk.
Check for the product name 'Lacosamide Tablets, 50mg, 60-count bottles' with NDC number 68462-678-60 and lot number 17240221. The expiration date is January 26, 2027.
Look for the NDC number 68462-678-60 and lot number 17240221 on the packaging.
Glenmark Pharmaceuticals is recalling 50mg Lacosamide tablets due to CGMP deviations in manufacturing.
Check for NDC number 68462-678-60 and lot number 17240221 with an expiration date of January 26, 2027.
The recall record does not specify a remedy, so contact Glenmark Pharmaceuticals for further instructions.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0337-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0337-2025 from Glenmark. 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.
