FDA-Drug2014-01-22Class II
PIMOZIDE Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 57844018701
Aidapak Services, LLC
Hazard
Labeling:Label Mixup; PIMOZIDE Tablet, 2 mg may be potentially mislabeled as DULoxetine HCl DR, Capsule, 20 mg, NDC 00002323560, Pedigree: AD30140_31, EXP: 5/7/2014.
Sold states
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Affected count
100 Tablets
Manufactured in
14301 Se 1st St, Vancouver, WA, United States
Products
PIMOZIDE Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 57844018701
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-633-2014Don't want to check this manually?
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