Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
buPROPion Hydrochloride Extended Release Tablets Recalled by American Health Packaging Due to Failed Stability Specifications; out of specification results at...
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 American Health Packaging directly.
Affected Products
buPROPion Hydrochloride Extended Release Tablets, USP 100 mg, 100 count carton, 10 blister cards of 10 individually blistered and labeled tablets, Rx only, Actavis South Atlantic LLC, Packaged and Distributed by: American Health Packaging, Columbus, OH --- NDC 68084-470-01
Quantity: 389 cartons
Why Was This Recalled?
Failed Stability Specifications; out of specification results at the 9 month stability time point for color, dissolution and related compounds.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About American Health Packaging
American Health Packaging has 56 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report