Glenmark Pharmaceuticals recalls 225mg extended-release capsules due to manufacturing deviations. This may affect safety in normal use. Check NDC# 68462-408-60 and lot # 17230819 for affected products.
CGMP Deviations
Glenmark is recalling 225mg extended-release propafenone capsules because of manufacturing deviations. This could pose safety risks if the product is used as intended.
CGMP deviations refer to failures in the manufacturing process that could affect product safety. Without specific details on the nature of the deviations, it's unclear how this impacts the product's safety in normal use.
People with prescriptions for this medication are affected. Those using the product without a prescription are not impacted, as it's Rx only.
Check for NDC# 68462-408-60 and lot # 17230819 on the product label. The product is only available by prescription and sold in 60-count bottles.
Look for NDC# 68462-408-60 and lot # 17230819 on the label to confirm if it's affected.
The recall is due to manufacturing deviations, but the official notice doesn't specify if the product is safe to use without action.
Check the product label for NDC# 68462-408-60 and lot # 17230819. This product is only available by prescription.
The recall notice doesn't specify a remedy, so there's no action required beyond checking if you have the product.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0315-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0315-2025 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.
