US Drug Recall Register
Class III · Low risk Terminated Initiated Jan 4, 2013 (14 years ago)

buPROPion Hydrochloride Extended - Release Tablets (XL) 300 mg, 30 tablet bottles, Rx…

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

Why it was recalled

Failed Dissolution Specifications; 8-hours for the 18-month stability testing point.

What was recalled

buPROPion Hydrochloride Extended - Release Tablets (XL) 300 mg, 30 tablet bottles, Rx Only, NDC 67767-142-30 Actavis Distributed by: Actavis South Atlantic LLC Sunrise, FL 33325 Packaged by by: America Health Packaging Columbus, OH 43217

Recalling firm
Actavis Pharmaceuticals
NDC code
67767-142-30
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-175-2013

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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