Aidapak Services, LLC recalls HYDROCHLOROTHIAZIDE Tablet, 12.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16729018201

Recalled January 22, 2014 · FDA recall D-525-2014 · Aidapak Services

Hazard

Labeling: Label Mixup; HYDROCHLOROTHIAZIDE Tablet, 12.5 mg may be potentially mislabeled as chlordiazePOXIDE HCl, Capsule, 25 mg, NDC 00555015902, Pedigree: AD46333_4, EXP: 5/16/2014. · FDA Class II

Units

100 Tablets

Sold at

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

Description

Labeling: Label Mixup; HYDROCHLOROTHIAZIDE Tablet, 12.5 mg may be potentially mislabeled as chlordiazePOXIDE HCl, Capsule, 25 mg, NDC 00555015902, Pedigree: AD46333_4, EXP: 5/16/2014.

Product

HYDROCHLOROTHIAZIDE Tablet, 12.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16729018201

Manufacturer(s)

Aidapak Services, LLC

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