Glenmark Pharmaceuticals recalls 50mg Voriconazole tablets due to CGMP deviations. This affects specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 50mg Voriconazole tablets that were manufactured with CGMP deviations. This means the product may not meet safety standards, so affected users should stop using it and contact the manufacturer.
CGMP deviations refer to failures in manufacturing quality control that could affect product safety. This means the tablets might not meet the required standards for safe use, though the exact risk is not specified in the recall.
Prescription users of Voriconazole 50mg tablets manufactured by Glenmark Pharmaceuticals Limited in India. Those with the specific lot number and expiration date are most at risk.
Check for the product name 'Voriconazole Tablets 50mg', 30-count bottle, and prescription label. Look for lot number 17231045 and expiration date April 25, 2025.
Discard the affected tablets immediately as they may not meet safety standards.
Voriconazole Tablets 50mg, 30-count bottle, prescription-only, manufactured by Glenmark Pharmaceuticals Limited in India.
Lot # 17231045, expiration date April 25, 2025.
Check the product label for the lot number 17231045 and expiration date April 25, 2025.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0319-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0319-2025 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.
