Glenmark Pharmaceuticals recalls 5mg Saxagliptin tablets (30-count and 90-count bottles) due to CGMP deviations. Rx-only medication with specific NDC numbers and expiration dates. Consumers should contact the manufacturer for details.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 5mg Saxagliptin tablets in 30-count and 90-count bottles due to manufacturing quality control issues. This recall affects prescription-only medication with specific product identifiers and expiration dates.
CGMP deviations refer to manufacturing quality control issues that could affect the safety and effectiveness of the medication. This means the tablets might not meet the required standards for a prescription drug, potentially leading to health risks if used improperly.
Prescription holders of the 5mg Saxagliptin tablets with NDC numbers 68462-727-30 or 68462-727-90. Individuals using these medications under a doctor's supervision are most at risk.
Check for the 5mg Saxagliptin tablets in 30-count or 90-count bottles with NDC numbers 68462-727-30 or 68462-727-90. These are prescription-only medications with specific expiration dates.
Reach out to Glenmark Pharmaceuticals Inc. USA for specific instructions on handling the recalled product.
The recall is due to CGMP deviations, which means the medication may not meet quality standards. Do not use until you get official guidance from the manufacturer.
The expiration dates vary: Nov-25 for some lots and Jun-26 for others, as listed in the recall notice.
Check for the NDC numbers 68462-727-30 or 68462-727-90 on the 30-count or 90-count bottles of 5mg Saxagliptin tablets.
We’ve drafted a message you can send Glenmark Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0332-2025 — Glenmark Pharmaceuticals Glenmark Pharmaceuticals Hello, I own a Glenmark Pharmaceuticals that is covered by recall D-0332-2025 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.
