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losartan latest bp drug recalled for contamination - Losartan Latest BP Drug Recalled for Contamination

Losartan Latest BP Drug Recalled for Contamination

Losartan Latest BP Drug Recalled for Contamination

Nov. 13, 2018 — Yet some other blood power drug has been recalled as a result of fears of impurities added through a lab in China.

Drug corporate Sandoz says it has recalled one lot of losartan potassium hydrochlorothiazide drugs. The impurity, referred to as NDEA, used to be discovered within the drug’s key element made through Zhejiang Huahai Pharmaceutical Co. in China.

NDEA is located naturally in sure meals, ingesting water, air air pollution, and commercial processes, and it’s going to reason most cancers, in step with the International Agency for Research on Cancer.

The recalled drug will also be recognized as Losartan Potassium Hydrochlorothiazide, 100-milligram and 25-milligram drugs in 1,000-count plastic bottles; NDC (National Drug Code) 0781-5207-10; Lot quantity JB8912; with an expiration date of 06/2020. This product used to be allotted national to vendors after Oct. 8.

This newest recall follows a number of others introduced since July, when the FDA introduced the recall of 5 separate valsartan blood power medicine over conceivable NDEA and NDMA contamination. Many extra have been introduced in August because the recall unfold to Canada and the European Union. And previous this month, a blood power drug referred to as irbesartan used to be recalled.

People with questions might touch Sandoz Inc. at 800-525-8747, Monday thru Friday from 8:30 a.m. to five p.m. ET, or e mail [email protected] Contact your physician or pharmacist to talk about choice remedies. Patients who’re on losartan will have to proceed taking their drugs, as they is also much more likely to be harmed if the remedy is stopped with out another.



Sources

FDA.gov: “Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Losartan Potassium and Hydrochlorothiazide Due to the Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in the Active Pharmaceutical Ingredient (API).”



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