HYDROXYCHLOROQUINE SULFATE Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63304029601

Recall Number: D-677-2014

Firm: Aidapak Services, LLC

Classification: Class II

Status: Terminated

Report Date: 20140122

Initiation Date: 20130702

Termination Date: 20140207

Reason for Recall

Labeling:Label Mixup; HYDROXYCHLOROQUINE SULFATE, Tablet, 200 mg may be potentially mislabeled as guanFACINE HCl, Tablet, 1 mg, NDC 00378116001, Pedigree: AD70629_7, EXP: 5/29/2014.

Product Description

HYDROXYCHLOROQUINE SULFATE Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63304029601

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Data source: openFDA · Updated regularly