US Drug Recall Register
Class III · Low risk Terminated Initiated Jul 31, 2013 (13 years ago)

BuPROPion Hydrochloride Extended-Release Tablets (XL), 300 mg, 30-count tablets per…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Dissolution Specifications: Dissolution test results at 8 hour time-point were above approved specification limits.

What was recalled

BuPROPion Hydrochloride Extended-Release Tablets (XL), 300 mg, 30-count tablets per bottle, Rx only, Distributed by: Actavis South Atlantic, LLC, Sunrise, FL 33325; Packaged by: American Health Packaging, Columbus, OH 43217, NDC 67767-142-30, UPC 3 67767-142-30 6.

Recalling firm
Actavis Inc
NDC code
67767-142-30
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-855-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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