Major Pharmaceuticals recalls 25mg chlorpromazine tablets due to potential presence of N-Nitroso Desmethyl Chlorpromazine above safe limits. This may pose health risks with long-term use. Consumers should contact the company for details.
CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit
Major Pharmaceuticals is recalling 25mg chlorpromazine tablets because they may contain unsafe levels of N-Nitroso Desmethyl Chlorpromazine. This chemical could pose health risks with long-term use, though the recall does not specify immediate danger.
The tablets may contain N-Nitroso Desmethyl Chlorpromazine at levels above the recommended intake limit. This chemical could pose health risks with long-term use, though the recall does not specify immediate danger.
Prescription patients using the 25mg chlorpromazine tablets with NDC 0904-7130-61. Those with specific medical conditions requiring long-term use may be at higher risk.
Check for the 25mg chlorpromazine tablets in a 100-tablet blister pack with NDC 0904-7130-61. The lot numbers N01954 (expiring 11/30/2025) and N02024 (expiring 02/28/2026) are also indicators.
Reach out to Major Pharmaceuticals for specific instructions on handling the recalled tablets.
The recall states the tablets may contain unsafe levels of N-Nitroso Desmethyl Chlorpromazine, but does not specify immediate danger. Consult your doctor for personalized advice.
Look for the NDC 0904-7130-61, 100-tablet blister pack, and lot numbers N01954 (expiring 11/30/2025) or N02024 (expiring 02/28/2026).
Contact Major Pharmaceuticals directly for specific instructions on handling the recalled tablets.
We’ve drafted a message you can send Major Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0010-2026 — Major Pharmaceuticals Major Pharmaceuticals Hello, I own a Major Pharmaceuticals that is covered by recall D-0010-2026 from Major 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.
