Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Losartan Potassium and Hydrochlorothiazide Due to the Detec

Budget101 Discussion List Archives Recalls Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Losartan Potassium and Hydrochlorothiazide Due to the Detec

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      budget

      Sandoz Inc. is voluntarily recalling one lot of Losartan Potassium Hydrochlorothiazide Tablets, USP 100mg/25mg to the consumer level. This product is being recalled due to the trace amount of an impurity, N-nitrosodiethylamine (ndea) contained in the api losartan, usp manufactured by zhejiang huahai pharmaceutical co.

      ltd. sandoz inc. losartan potassium hydrochlorothiazide product is manufactured by lek pharmaceuticals dd, ljubljana, slovenia.

      this impurity, which is a substance that occurs naturally in certain foods, drinking water, air pollution, and industrial processes, has been classified as a probable human carcinogen as per international agency for research on cancer (iarc).

      Read More…

      This notice provided by Budget101.com

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Budget101 Discussion List Archives Recalls Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Losartan Potassium and Hydrochlorothiazide Due to the Detec