Glenmark Pharmaceuticals recalls 275mg Naproxen Sodium Tablets due to CGMP deviations. These prescription pain relievers may have quality issues affecting safety. Check NDC 68462-178-01 for affected lots.
CGMP Deviations
Glenmark Pharmaceuticals is recalling prescription Naproxen Sodium Tablets (275mg, 100 tablets) because of manufacturing quality control issues. This recall affects people who have these specific tablets and may pose a risk to safety if the tablets do not meet quality standards.
The recall is for CGMP (Current Good Manufacturing Practices) deviations, which means the tablets may not meet the required quality standards during production. This could potentially affect the safety and effectiveness of the medication.
Prescription users of Naproxen Sodium Tablets (275mg, 100 tablets) with NDC 68462-178-01. People who have the specific lots listed in the recall are most at risk.
Check for the NDC code 68462-178-01 on the product packaging. The affected lots include 29190087, 29190088, 29190089, 29200077, and 29200078 with expiration dates up to November 30, 2022.
Look for the NDC code 68462-178-01 on the tablet packaging to confirm if it's affected.
The product was recalled due to CGMP deviations, which means there may be quality issues affecting safety.
Affected lots include 29190087, 29190088, 29190089, 29200077, and 29200078 with expiration dates up to November 30, 2022.
The recall does not specify a stop-use instruction, so you do not need to stop using them immediately.
We’ve drafted a message you can send Glenmark Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0821-2021 — Glenmark Pharmaceuticals Glenmark Pharmaceuticals Hello, I own a Glenmark Pharmaceuticals that is covered by recall D-0821-2021 from Glenmark Pharmaceuticals. 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.
