Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
buPROPion Hydrochloride Extended-Release Tablets Recalled by Amerisource Health Services Due to Failed dissolution specifications - the out of specification...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Amerisource Health Services directly.
Affected Products
buPROPion Hydrochloride Extended-Release Tablets, USP (XL), 300mg, 500-count bottle, Rx only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India For BluePoint Laboratories, NDC 68001-264-03
Quantity: 2626 bottles
Why Was This Recalled?
Failed dissolution specifications - the out of specification result for dissolution was identified during 3 month stability testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Amerisource Health Services
Amerisource Health Services has 23 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report