Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
BuPROPion HCL Tablets Recalled by Mckesson Packaging Services Due to Failed Moisture Limits: Product tested out-of-specification for moisture...
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 Mckesson Packaging Services directly.
Affected Products
BuPROPion HCL Tablets, USP, 75 mg, packaged as UD 100 tablets (10x10), Rx Only, Mfg by: Sandoz Inc., 508 Carnegie Center, Suite 400, Princeton, NJ 08805, NDC: 63739-706-10
Quantity: 942 cartons
Why Was This Recalled?
Failed Moisture Limits: Product tested out-of-specification for moisture content.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mckesson Packaging Services
Mckesson Packaging Services has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report