Heritage Pharmaceuticals recalls 10mg Desipramine tablets due to N-Nitroso impurity exceeding safe levels. Rx-only medication with specific NDC number. No remedy stated in official notice.
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
Heritage Pharmaceuticals is recalling 100-count 10mg Desipramine Hydrochloride tablets (NDC 23155-578-01) because they contain an impurity that could exceed safe daily intake levels. This is a prescription-only medication that may pose health risks if taken without proper medical supervision.
The tablets contain N-Nitroso Desipramine impurities that exceed the permissible acceptable daily intake level. This impurity could potentially cause health issues if taken in amounts exceeding safe limits, though the exact risk level isn't specified in the recall notice.
Prescription patients who have the specific 100-count 10mg Desipramine tablets with NDC 23155-578-01. Those with medical conditions requiring this medication are most at risk.
Look for the 100-count bottle labeled 'Desipramine Hydrochloride Tablets, USP, 10 mg' with NDC code 23155-578-01. The product is prescription-only and manufactured by USV for Avet Pharmaceuticals.
Verify the NDC code 23155-578-01 on the bottle to confirm it's the recalled product.
The recall states the product contains impurities exceeding safe intake levels, but no specific remedy is provided. Prescription patients should consult their doctor.
Check for the NDC code 23155-578-01 on the 100-count 10mg Desipramine Hydrochloride tablets.
The official recall notice does not specify any action steps. Prescription patients should contact their doctor for guidance.
We’ve drafted a message you can send Heritage Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0107-2026 — Heritage Pharmaceuticals Heritage Pharmaceuticals Hello, I own a Heritage Pharmaceuticals that is covered by recall D-0107-2026 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.
