Lupin Pharmaceuticals recalls 50mg Losartan Potassium Tablets with AZIDO impurities above safe limits. Rx-only medication from India manufactured for US distribution.
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Lupin Pharmaceuticals is recalling 50mg Losartan Potassium Tablets due to unsafe levels of an AZIDO impurity. This medication poses a potential health risk if taken as prescribed.
The recall is for AZIDO impurities found in the medication that exceed acceptable safety limits. This chemical could potentially cause health issues when taken as directed.
People who have the recalled 50mg Losartan Potassium Tablets (90-count or 1000-count bottles) from Lupin Pharmaceuticals. Those with hypertension requiring this medication are most at risk.
Check for 50mg Losartan Potassium Tablets in 90-count or 1000-count bottles with NDC numbers 68180-377-03 or 68180-377-09. These are prescription-only medications manufactured by Lupin Pharmaceuticals.
Look for the NDC numbers 68180-377-03 or 68180-377-09 on the bottle label to confirm if it's recalled.
The recall indicates unsafe levels of AZIDO impurities, so it is not safe to take as prescribed.
The recall does not specify a remedy, so contact your doctor or pharmacist for guidance.
The recall lists multiple expiration dates from November 2022 to March 2023, but the exact date depends on the batch.
We’ve drafted a message you can send Lupin to request your refund or repair — edit it as you like.
Subject: Recall D-0839-2022 — Lupin Lupin Hello, I own a Lupin that is covered by recall D-0839-2022 from Lupin. 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.
