Glenmark Pharmaceuticals recalls 225mg Propafenone Extended-Release Capsules due to CGMP deviations. Rx-only medication with specific lot numbers and expiration dates.
CGMP Deviations
Glenmark is recalling 225mg Propafenone Hydrochloride Extended-Release Capsules because of manufacturing quality control issues. This recall affects prescription-only medication with specific lot numbers and expiration dates.
CGMP deviations refer to manufacturing quality control failures that could affect the safety and effectiveness of the medication. This means the product might not be as intended, potentially leading to health risks if used without proper quality assurance.
Prescription patients who have the specific lot number (17230819) of 225mg Propafenone Extended-Release Capsules. Those with the medication expired by March 2025 are at risk.
Check for the lot number 17230819 on the bottle. The product expires March 2025. This is a prescription-only medication with NDC code 16714-825-01.
Look for the lot number 17230819 and expiration date of March 2025 on the bottle.
The recall is due to CGMP deviations, which means the product may not meet safety standards. Consult your doctor before using.
Check the lot number and expiration date. If it matches the recalled batch, contact your doctor for guidance.
Look for the lot number 17230819 and expiration date of March 2025 on the bottle. This is a prescription-only medication with NDC code 16714-825-01.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0351-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0351-2025 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.
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.