RemedyRepack Inc. recalls Losartan HCTZ 100/25 mg, 90 count bottles NDC# 70518-2578-00 Repackaged NDC Original NDC # 68180-0217-09
Recalled June 1, 2022 · FDA recall D-0886-2022 · RemedyRepack
Hazard
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits. · FDA Class II
Units
26/90 count bottles = 2,340 tablets
Sold at
Product was distributed to FL, SC and VA
Description
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.
Product
Losartan HCTZ 100/25 mg, 90 count bottles NDC# 70518-2578-00 Repackaged NDC Original NDC # 68180-0217-09
Manufacturer(s)
RemedyRepack Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →