Glenmark Pharmaceuticals recalls 120mg Diltiazem Hydrochloride Extended-Release Capsules due to CGMP deviations. Affected units have specific NDC and lot numbers. Consumers should contact the company for details.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 120mg Diltiazem Hydrochloride Extended-Release Capsules 100-count bottles because of manufacturing quality control issues. This recall affects people who have these specific capsules and may pose a risk to their health if the product is used without addressing the issue.
CGMP deviations refer to manufacturing quality control failures that could lead to unsafe products. While the exact nature of the deviation isn't specified, such issues can potentially cause harmful effects if the medication is not properly controlled during production.
People who have the 120mg Diltiazem Hydrochloride Extended-Release Capsules 100-count bottles with NDC 68462-562-01 and lot number 17241067 are affected. Those taking this medication for blood pressure or other conditions are most at risk.
Check for the NDC number 68462-562-01 and lot number 17241067 on the bottle. The product is a 100-count bottle of 120mg Diltiazem Hydrochloride Extended-Release Capsules, labeled as Rx only.
Look for the NDC number 68462-562-01 and lot number 17241067 on the bottle.
The recall record states there were CGMP deviations, but does not specify if the product is safe to use. Consumers should contact Glenmark for details.
The recall record does not provide specific action steps. Consumers should contact Glenmark Pharmaceuticals for guidance.
Check for the NDC number 68462-562-01 and lot number 17241067 on the bottle. The product is a 100-count bottle of 120mg Diltiazem Hydrochloride Extended-Release Capsules, labeled as Rx only.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0342-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0342-2025 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.
