Losartan potassium tablets
Official-information notice / 官方信息说明
This page organizes fields from the named agency record. It is not medical, legal, or food-safety advice. Always compare your package with the official notice.
Official record details
官方记录详情：以原始机构公告为准
Recall number / 召回编号
fda-alert:2019-06-11:GSMS Inc.:Losartan potassium tablets
Classification / 风险等级
Other / 其他
Published / 发布时间
2019-06-11
Recalling firm / 召回企业
Teva Pharmaceuticals USA, Inc.
Product description / 产品描述
Losartan potassium tablets
Product code / 产品代码
Not provided in the official record
Code information / 批次与代码信息
Not provided in the official record
Product quantity / 产品数量
Not provided in the official record
Distribution / 销售地区
Not provided in the official record
Reason for recall / 召回原因
Detection of an impurity – N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)
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Last synchronized: 2019-06-11. Recall Radar does not replace agency guidance.