Glenmark Pharmaceuticals recalls 14mg Terif: CGMP deviations in manufacturing. Rx-only tablets may be unsafe. Check NDC# 68462-424-30 and lot # 17232462 for affected units.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 14mg Teriflunomide tablets due to manufacturing deviations. This recall affects prescription-only medication that may pose safety risks if used improperly.
CGMP deviations refer to failures in quality control during manufacturing. This could mean the tablets do not meet safety standards, potentially leading to unsafe medication. However, the exact risk is not specified in the recall notice.
Prescription patients using Teriflunomide tablets manufactured by Glenmark Pharmaceuticals Limited in India. Those with the specific NDC# 68462-424-30 and lot # 17232462 are most at risk.
Check for the NDC code 68462-424-30 and lot number 17232462 on the product label. The tablets are prescription-only and sold in 30-count bottles.
Look for NDC# 68462-424-30 and lot # 17232462 on the tablet packaging.
The recall states there were CGMP deviations, but does not specify if the medication is safe. Consult your healthcare provider for advice.
Check the NDC# 68462-424-30 and lot # 17232462 on the product label. This is the specific batch affected by the recall.
The recall does not provide a remedy, so contact your healthcare provider for guidance on next steps.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0334-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0334-2025 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.