Perrigo Company PLC recalls Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 95 tablets per bottle. [Brand, NDC] NDC Basic Care: 0113-
Recalled March 25, 2020 · FDA recall D-1026-2020 · Perrigo Company
Hazard
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine. · FDA Class II
Sold at
Nationwide USA
Description
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Product
Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 95 tablets per bottle. [Brand, NDC] NDC Basic Care: 0113-7852-01; NDC Berkley Jensen: 68391-852-56; NDC: CVS Health: 59779-540-01; NDC DG Health: 55910-011-01; NDC Kirkland: 63981-852-56; NDC Kroger: 30142-600-56; NDC Meijer: 41250-852-01; NDC Rite Aid: 11822-0852-4; NDC Walgreens: 0363-0852-01
Manufacturer(s)
Perrigo Company PLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →