Glenmark Pharmaceuticals recalls 200mg Rufinamide tablets due to CGMP deviations. This affects 120-count bottles with specific lot numbers. Consumers should contact the company for details.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 200mg Rufinamide 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 quality control issues during manufacturing that could affect the safety and effectiveness of the medication. This means the tablets might not meet the required standards for safe use.
Prescription patients who have the 200mg Rufinamide tablets with the specific lot numbers and expiration dates listed in the recall. Those who have the product are most at risk.
Check for the 200mg Rufinamide tablets in a 120-count bottle with the lot number 17231643 or 17231644 and expiration dates of July 2025.
Reach out to Glenmark Pharmaceuticals Inc. USA for specific instructions on handling the recalled product.
Glenmark Pharmaceuticals is recalling 200mg Rufinamide tablets due to CGMP deviations in manufacturing.
Look for the 200mg Rufinamide tablets in a 120-count bottle with lot numbers 17231643 or 17231644 and expiration dates of July 2025.
Contact Glenmark Pharmaceuticals Inc. USA for specific instructions on handling the recalled product.
We’ve drafted a message you can send Glenmark Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0323-2025 — Glenmark Pharmaceuticals Glenmark Pharmaceuticals Hello, I own a Glenmark Pharmaceuticals that is covered by recall D-0323-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
