FDA-Drug2014-01-22Class II
guaiFENesin ER Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824000834
Aidapak Services, LLC
Hazard
Labeling:Label Mixup; guaiFENesin ER, Tablet, 600 mg may be potentially mislabeled as PRENATAL MULTIVITAMIN/ MULTIMINERAL, Tablet, NDC 51991056601, Pedigree: AD62829_18, EXP: 5/24/2014; guaiFENesin ER, Tablet, 600 mg, NDC 63824000834, Pedigree: AD62834_4, EXP: 5/24/2014; diphenhydrAMINE HCl, Tablet, 25 mg, NDC 00904555159, Pedigree: W003513, EXP: 6/21/2014; DOCUSATE SODIUM, Capsule, 250 mg,
Sold states
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Affected count
480 Tablets
Manufactured in
14301 Se 1st St, Vancouver, WA, United States
Products
guaiFENesin ER Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824000834
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-683-2014Don't want to check this manually?
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