FDA-Drug2014-01-22Class II
FAMOTIDINE Tablet, 20 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 16714036104
Aidapak Services, LLC
Hazard
Labeling: Label Mixup; FAMOTIDINE Tablet, 20 mg may be potentially mislabeled as CARVEDILOL PHOSPHATE ER, Capsule, 20 mg, NDC 00007337113, Pedigree: W003225, EXP: 6/17/2014; DULoxetine HCl DR, Capsule, 20 mg, NDC 00002323560, Pedigree: W003506, EXP: 6/21/2014; FAMOTIDINE, Tablet, 20 mg, NDC 16714036104, Pedigree: W003507, EXP: 6/21/2014; MYCOPHENOLATE MOFETIL, Capsule, 250 mg, NDC 0037822500
Sold states
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Affected count
700 Tablets
Manufactured in
14301 Se 1st St, Vancouver, WA, United States
Products
FAMOTIDINE Tablet, 20 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 16714036104
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-518-2014Don't want to check this manually?
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