Ascend Minocycline 115mg Recall
Minocycline Hydrochloride Extended-Release Tablets, USP, 115 mg, 30-count bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA.
Updated June 1, 2026
Ascend Laboratories is recalling Minocycline Hydrochloride Extended-Release Tablets, USP, 115 mg because some bottles failed to meet dissolution specifications during testing, meaning the medication may not dissolve and release properly in the body.
Is the Ascend Laboratories, LLC recalled? Yes. This product was recalled by FDA on June 1, 2026. Details below.
What is recalled
Minocycline Hydrochloride Extended-Release Tablets, USP, 115 mg, 30-count bottle, NDC 67877-644-30, manufactured by Alkem Laboratories Ltd., India, and distributed by Ascend Laboratories, LLC, Parsippany, NJ 07054. Rx Only.
Am I affected
You're affected if your prescription medication bottle is labeled Minocycline Hydrochloride Extended-Release Tablets, 115 mg, with NDC 67877-644-30, and you received it from Ascend Laboratories.
What to do right now
Contact your pharmacist or doctor to discuss whether your medication is affected and what to do next. Do not stop taking your medication without speaking to your healthcare provider first.
The hazard
Failed Dissolution Specifications: An out-of-specification (OOS) result was observed during the 9th month of dissolution test analysis
Brands affected
- Source
- FDA
- Category
- Drugs & Medications
- Recall ID
- fda-D-0597-2026
- Classification
- Class II
- Recalled
- June 1, 2026
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