Amerisource Health recalls buPRODIA 150mg extended-release tablets that dissolve faster than intended. This may affect medication effectiveness. Check your carton for lot number 1017343.
Failed Dissolution Specifications; the product is dissolving faster than the specified limits.
Amerisource Health is recalling buPRODIA 150mg extended-release tablets that dissolve faster than specified. This could lead to inconsistent medication levels in the body.
The tablets dissolve too quickly, which may cause inconsistent medication levels in the body. This could lead to ineffective treatment for depression or anxiety.
People who have the specific lot number 1017343 of buPRODIA 150mg tablets. Those taking this medication for depression or anxiety are most at risk.
Look for the carton labeled 'buPROPion Hydrochloride Extended-release Tablets USP (XL) Once-Daily, 150 mg, 100 Tablets (10 x 10) per carton'. Check the lot number on the carton, which is 1017343 for this recall.
Look for the lot number 1017343 on the carton of buPRODIA tablets.
The recall is due to faster dissolving than specified, which may affect medication effectiveness. It is not safe to use as intended.
Check the lot number on the carton. If it is 1017343, stop using it and contact Amerisource Health.
The recall record does not specify a replacement process.
We’ve drafted a message you can send Amerisource Health to request your refund or repair — edit it as you like.
Subject: Recall D-0590-2024 — Amerisource Health Amerisource Health Hello, I own a Amerisource Health that is covered by recall D-0590-2024 from Amerisource Health. 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.
