Glenmark Pharmaceuticals recalls 100mg Atomoxetine Capsules due to N-Nitroso impurity exceeding FDA limits. Affected lots manufactured in Memphis, TN. Stop using if you have these specific lot numbers.
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
Glenmark Pharmaceuticals is recalling 100mg Atomoxetine Capsules that may contain an impurity exceeding FDA safety limits. This could pose a health risk, so affected users should stop using the product and contact their doctor.
The capsules contain N-Nitroso Atomoxetine impurities above the FDA's recommended limit. This impurity could potentially cause health issues, though the exact risk level is not specified in the recall.
People with prescriptions for Atomoxetine Capsules (for ADHD) who received the specific lot numbers listed in the recall. Those with the capsules manufactured in Memphis, TN by Northstar Rx LLC are most at risk.
Check the lot numbers on the bottle: 19233270, 19233278, 19233285 (expiring 7/2025), 19233806 (expiring 8/2025), 19240954 (expiring 2/2026), and 19241854 (expiring 4/2026). These are the only affected lots.
Look for the lot numbers listed in the recall: 19233270, 19233278, 19233285, 19233806, 19240954, or 19241854.
If you have the recalled lot numbers, talk to your doctor about stopping use and possible alternatives.
The capsules contain N-Nitroso Atomoxetine impurities above the FDA's recommended limit, which could pose a health risk.
Check the lot numbers on the bottle. If you have one of the listed lot numbers, stop using it and contact your doctor.
No, only the specific lot numbers listed in the recall are affected.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0244-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0244-2025 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.
