US Drug Recall Register
Class III · Low risk Terminated Initiated Mar 18, 2013 (13 years ago)

Oxcarbazepine Tablets, 150 mg, packaged in a) 10 x 10 count Unit-Dose Tablets in blisters…

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

Why it was recalled

SubPotent Drug: The firm discovered out of specification results for assay and the extended investigation revealed the potential for lower weight tablets.

What was recalled

Oxcarbazepine Tablets, 150 mg, packaged in a) 10 x 10 count Unit-Dose Tablets in blisters packaged in a carton (NDC 0054-0097-20) and b) 100-count bottle (NDC 0054-0097-25), Rx only, Roxane Laboratories, Inc., Columbus, Ohio 43216

Recalling firm
Boehringer Ingelheim Roxane Inc
NDC code
0054-0097-20
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-343-2014

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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