Glenmark Pharmaceuticals recalls 0.4mg nitroglycerin sublingual tablets due to CGMP deviations. Affected lots manufactured in India with specific expiration dates. Consumers should contact the company for details.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 0.4mg nitroglycerin sublingual tablets because of manufacturing quality control issues. This recall affects specific lots with expiration dates in August and September 2025. The issue could lead to improper medication strength or safety risks if the tablets are not manufactured correctly.
CGMP deviations mean the manufacturing process did not meet quality standards. This could result in tablets that are not the correct strength or may be unsafe for use, potentially causing ineffective treatment or adverse effects.
People with prescriptions for nitroglycerin sublingual tablets who own the specific lot numbers mentioned in the recall. Those with heart conditions or using the medication for chest pain are at higher risk.
Check the product label for the lot number (17232024, 17232071, or 17232072) and expiration dates (August 2025 or September 2025). The product is a 100-count carton of 0.4mg nitroglycerin sublingual tablets, prescription-only.
Look for the lot number (17232024, 17232071, or 17232072) and expiration dates on the packaging.
The recall is due to CGMP deviations, which means the manufacturing process did not meet quality standards. This could result in tablets that are not the correct strength or may be unsafe for use.
Check the product label for the lot number (17232024, 17232071, or 17232072) and expiration dates (August 2025 or September 2025). The product is a 100-count carton of 0.4mg nitroglycerin sublingual tablets, prescription-only.
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-0324-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0324-2025 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.
