Glenmark Pharmaceuticals recalls 600mg gabapentin tablets (500-count bottles) due to CGMP deviations. These tablets may not meet quality standards. Consumers should check lot numbers and expiration dates on packaging.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 600mg gabapentin tablets in 500-count bottles that were manufactured with CGMP deviations. This means the tablets may not meet quality standards, which could affect safety and effectiveness.
CGMP deviations refer to failures in the manufacturing process that could result in the tablets not meeting quality standards. This might lead to inconsistent drug strength or safety issues, though the specific risks are not clearly described in the recall notice.
Prescription holders of 600mg gabapentin tablets (500-count bottles) manufactured by Glenmark Pharmaceuticals Limited in India for Glenmark Pharmaceuticals Inc. in the US are affected. People taking this medication for conditions like neuropathic pain or seizures are most at risk.
Check the product label for the lot number (e.g., 17231015) and expiration date (e.g., Apr-25). The tablets are 600mg, 500-count bottles, and are prescription-only.
Look for the lot number (e.g., 17231015) and expiration date on the packaging.
The recall is due to CGMP deviations during manufacturing, which may affect the quality and safety of the tablets.
Check the product label for the lot number (e.g., 17231015) and expiration date (e.g., Apr-25). The product is 600mg gabapentin tablets in 500-count bottles.
The recall notice does not specify a remedy, so contact your doctor or pharmacist for guidance.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0320-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0320-2025 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.
