Amerisource Health Services recalls buPROPion Hydrochloride Extended-Release Tablets, USP (XL), 300mg, 500-count bottle, Rx only, Manufactured by: Cadila
Failed dissolution specifications - the out of specification result for dissolution was identified during 3 month stability testing.
Recall notice
Failed dissolution specifications - the out of specification result for dissolution was identified during 3 month stability testing.
Contact the company & request your remedy
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We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
Source Page by GovInfoNow · govinfonow.com/recall/42496-amerisource-health-services-recalls-bupropion-hydrochloride-extended-release-tablets-usp · Recall date August 4, 2016 · FDA enforcement record: FDA #D-1501-2016
Cite this page
“Amerisource Health Services recalls buPROPion Hydrochloride Extended-Release Tablets, USP (XL), 300mg, 500-count bottle, Rx only, Manufactured by: Cadila.” GovInfoNow, recall dated August 4, 2016. https://govinfonow.com/recall/42496-amerisource-health-services-recalls-bupropion-hydrochloride-extended-release-tablets-usp. Based on FDA recall #D-1501-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1501-2016%22&limit=1).
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Contact Amerisource Health Services
We’ve drafted a message you can send Amerisource Health Services to request your refund or repair — edit it as you like.
Subject: Recall D-1501-2016 — Amerisource Health Services Amerisource Health Services recalls buPROPion Hydrochloride Extended-Re Hello, I own a Amerisource Health Services recalls buPROPion Hydrochloride Extended-Release Tablets, USP (XL), 300mg, 500-count bottle, Rx only, Manufactured by: Cadila that is covered by recall D-1501-2016 from Amerisource Health Services. 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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Where this comes from
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.
- Official source: FDA Recall #D-1501-2016 (August 4, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1501-2016 to see it in context.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
