Ascend Laboratories recalls 115mg Minocycline Hydrochloride Extended-Release Tablets due to failed dissolution test. This may affect medication effectiveness. Check NDC 67877-644-30 and lot numbers for affected products.
Failed Dissolution Specifications: An out-of-specification (OOS) result was observed during the 9th month of dissolution test analysis
Ascend Laboratories is recalling 115mg Minocycline Hydrochloride Extended-Release Tablets because they failed a dissolution test. This could mean the medication doesn't work as intended. People with prescriptions for this product should check their NDC number and lot date.
The tablets failed a dissolution test during the 9th month of analysis. This suggests the medication may not release properly in the body, potentially reducing effectiveness. However, the recall does not indicate immediate harm or injury.
Prescription holders of the 115mg Minocycline Hydrochloride Extended-Release Tablets with NDC 67877-644-30. Patients who have been prescribed this medication are most at risk.
Check for the NDC number 67877-644-30 and lot number 25141635 on the bottle. The product is a prescription-only 115mg tablet with 30 tablets per bottle.
Look for NDC 67877-644-30 and lot number 25141635 on the bottle label.
The recall indicates a failed dissolution test, but the product is not unsafe to use. It may not work as intended, so patients should contact their doctor.
Check the NDC number and lot number on the bottle. If it matches the recalled product, contact your doctor for alternative medication.
Look for NDC 67877-644-30 and lot number 25141635 on the bottle label. The product is prescription-only and distributed by Ascend Laboratories.
We’ve drafted a message you can send Ascend Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0597-2026 — Ascend Laboratories Ascend Laboratories Hello, I own a Ascend Laboratories that is covered by recall D-0597-2026 from Ascend Laboratories. 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.
