Aidapak Services, LLC recalls OXcarbazepine Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62756018588

Recalled January 22, 2014 · FDA recall D-674-2014 · Aidapak Services

Hazard

Labeling:Label Mixup; OXcarbazepine Tablet, 600 mg may be potentially mislabeled as LACTASE ENZYME, Tablet, 3000 units, NDC 24385014976, Pedigree: AD30028_25, EXP: 5/7/2014. · FDA Class II

Units

100 Tablets

Sold at

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

Description

Labeling:Label Mixup; OXcarbazepine Tablet, 600 mg may be potentially mislabeled as LACTASE ENZYME, Tablet, 3000 units, NDC 24385014976, Pedigree: AD30028_25, EXP: 5/7/2014.

Product

OXcarbazepine Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62756018588

Manufacturer(s)

Aidapak Services, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →