Glenmark Pharmaceuticals recalls 0.3mg nitroglycerin sublingual tablets due to CGMP deviations. Affected lots expire Nov 2025. Consumers should contact for details.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 0.3mg nitroglycerin sublingual tablets that were manufactured with CGMP deviations. This recall means the tablets may not meet quality standards, which could affect safety and effectiveness.
CGMP deviations refer to quality control issues during manufacturing. These deviations could mean the tablets don't meet safety and effectiveness standards, potentially causing harm if used improperly.
People who own or use the recalled nitroglycerin tablets are affected. Those with heart conditions or using nitroglycerin for angina are at higher risk.
Check for the product name 'Nitroglycerin Sublingual Tablets 0.3MG, 100-count bottles' with lot numbers 17232361, 17240037, or 17240038. The expiration dates are November 2025 or December 2025.
Look for the lot numbers 17232361, 17240037, or 17240038 on the packaging.
The recall is due to CGMP deviations during manufacturing, which could affect the quality and safety of the tablets.
Check for the lot numbers 17232361, 17240037, or 17240038 on the packaging of the 0.3mg nitroglycerin sublingual tablets.
The recall record does not specify a remedy, so contact Glenmark Pharmaceuticals for further instructions.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0331-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0331-2025 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.
