Major Pharmaceuticals recalls 200mg chlorpromazine tablets due to potential presence of N-Nitroso Desmethyl Chlorpromazine above safe limits. This may pose health risks with improper use. Contact for return instructions.
CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit
Major Pharmaceuticals is recalling 200mg chlorpromazine tablets that may contain unsafe levels of N-Nitroso Desmethyl Chlorpromazine. This chemical could pose health risks if taken in amounts exceeding safe limits.
The tablets may contain N-Nitroso Desmethyl Chlorpromazine levels above the recommended intake limit. This chemical could pose health risks if taken in amounts exceeding safe limits. The hazard is related to potential chemical contamination during manufacturing.
Prescription users of Major Chlorpromazine 200mg tablets with NDC 0904-7133-61. Patients who have taken these tablets since the product was distributed are most at risk.
Check for the 200mg chlorpromazine tablets in a 10x10 blister pack with NDC 0904-7133-61. The product was distributed with specific lot numbers: N01928 (expiring 09/30/2025), N02008 (expiring 03/21/2026), and N02071 (expiring 02/28/2026).
Identify the NDC code 0904-7133-61 and lot numbers N01928, N02008, or N02071 on the blister pack.
The tablets may contain N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit, which could pose health risks if taken in amounts exceeding safe limits.
Check for the NDC code 0904-7133-61 and lot numbers N01928 (expiring 09/30/2025), N02008 (expiring 03/21/2026), or N02071 (expiring 02/28/2026) on the blister pack.
The recall record does not specify a remedy, so contact Major Pharmaceuticals directly for instructions.
We’ve drafted a message you can send Major Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0013-2026 — Major Pharmaceuticals Major Pharmaceuticals Hello, I own a Major Pharmaceuticals that is covered by recall D-0013-2026 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.
