Glenmark Pharmaceuticals recalls 200mg Voriconazole tablets due to manufacturing deviations. Affected lots have specific expiration dates and NDC numbers. Consumers should check their product details and contact the manufacturer for guidance.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 200mg Voriconazole tablets that were manufactured with CGMP (current good manufacturing practice) deviations. This recall affects specific lots with particular expiration dates and NDC numbers. The issue could lead to unsafe drug quality, but the recall does not specify immediate health risks or injuries.
CGMP deviations during manufacturing could result in unsafe drug quality. This means the medication might not be effective or could cause adverse reactions when taken. However, the recall does not specify the exact nature of the deviation or potential health impacts.
Prescription patients who have the specific 200mg Voriconazole tablets with the listed NDC number and lot numbers. Patients using these medications for fungal infections are most at risk due to potential quality issues.
Check for the NDC number 68462-573-30 on the product label. Look for specific lot numbers like 17230853, 17231271, 17231300, 17242050, 17231046, 17241156, 17241388, or 17241800. The product expires between April 2025 and October 2026.
Look for the NDC number 68462-573-30 and specific lot numbers listed in the recall.
The recall states there were CGMP deviations, but does not specify if the medication is unsafe. Patients should not use the affected lots until the manufacturer provides further guidance.
The recall does not specify a remedy, so contact Glenmark Pharmaceuticals Inc. USA for instructions on what to do with the product.
Check the NDC number 68462-573-30 and lot numbers listed in the recall description. The product expires between April 2025 and October 2026.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0318-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0318-2025 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.
