Heritage Pharmaceuticals recalls 75mg Desipramine tablets with N-Nitroso impurity exceeding safe levels. Rx-only medication from USV, manufactured in India. No remedy stated in recall notice.
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
Heritage Pharmaceuticals is recalling 75mg Desipramine Hydrochloride tablets that contain an impurity (N-Nitroso Desipramine) exceeding safe levels. This could pose a health risk with long-term use, though the recall does not specify a remedy.
The tablets contain N-Nitroso Desipramine impurities that exceed the permissible acceptable daily intake level. This impurity could potentially cause health issues with long-term use, though the exact risk is not specified in the recall notice.
Prescription medication users who have the specific 75mg Desipramine tablets with NDC 23155-581-01. People taking this medication for depression or other conditions are most at risk.
Check for the 75mg Desipramine Hydrochloride tablets with NDC 23155-581-01. The product was manufactured by USV Private Limited in Daman, India, and distributed by Avet Pharmaceuticals Inc. in New Jersey.
Look for the NDC code 23155-581-01 on the tablet packaging to confirm if it's recalled.
The recall states the impurity level exceeds permissible safe intake, but does not specify if it's safe for short-term use. Consult your doctor for advice.
The recall notice does not provide a remedy, so contact your doctor or pharmacist for guidance.
Check for the NDC code 23155-581-01 on the packaging. The product was manufactured by USV in Daman, India, and distributed by Avet Pharmaceuticals in New Jersey.
We’ve drafted a message you can send Heritage Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0110-2026 — Heritage Pharmaceuticals Heritage Pharmaceuticals Hello, I own a Heritage Pharmaceuticals that is covered by recall D-0110-2026 from Heritage 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.
