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On April 24, the company recalled an additional lot of 50mg losartan tablets.
The losartan used as an active ingredient in the medicine was found to contain N-Nitrosodiethylamine (NDEA), classified as a probable carcinogen . Update [11/9/2018] FDA is alerting patients and health care professionals to Sandoz’s voluntary recall of one lot – JB8912 – of losartan potassium and hydrochlorothiazide 100mg/25mg tablets, that contain losartan, an angiotensin II receptor blocker (ARB), and hydrochlorothiazide, a diuretic, used in combination for the treatment of hypertension. Torrent Pharmaceuticals Limited has expanded its voluntary recall of Losartan potassium tablets USP to include 6 lots of Losartan potassium and hydrochlorothiazide tablets, USP. 50mg, which are used to control blood pressure.The company initiated the recall after its own investigation discovered impurities within the medicine.The losartan used as an active ingredient in the medicine was found to contain N-Nitrosodiethylamine (NDEA), classified as a The agency also stated that it has strengthened its random testing procedure and has introduced requirements for the industry to conduct its own ‘self-inspections’.Sin Guan was prompted to begin its tests after the discovery of contaminated valsartan products by the European Medicines Agency After the initial recall of valsartan produced by Chinese manufacturer, Zhejiang Huahai, the investigation spread further to impact a Copyright - Unless otherwise stated all contents of this web site are © 2020 - William Reed Business Media Ltd - All Rights Reserved - Full details for the use of materials on this site can be found in the The drugs were made in India and distributed by Heritage Pharmaceuticals of East Brunswick, NJ. The presented program is laid out as integrated Drug Substance, Particle Engineering and Drug Product services, enabling drug substance and drug product... In April, the agency released a list of 40 blood pressure medications it says are free from contamination. About 40% of finished medications are made overseas, the Government Accountability Office says. Golden State re-packages the tablets under its own label for retail sale. On March 1, 2019, Camber Pharmaceuticals announced a recall affecting 87 lots of 25 mg, 50 mg and 100 mg losartan tablets.On March 15, 2019, Legacy Pharmaceuticals Packaging announced a voluntary recall of three repackaged lots of 50 mg of losartan tablets. Stress has been called the ‘health epidemic of the 21st century’ by the World Health Organization. The recall was issued due to the detection of trace amounts of an unexpected impurity found in an active pharmaceutical ingredient (API) manufactured by Hetero Labs Limited. Contract manufacturers are required to heavily invest in building new facilities. Macleods on June 26 also recalled 32 lots of losartan potassium including two lots of 50 mg tablets and losartan potassium/hydrochlorothiazide tablets, including 12 lots of 50 mg/12.5 mg strength, three lots of 100 mg/12.5 mg and 15 lots of 100 mg/25 mg strength. Camber Pharmaceuticals on Feb. 28 recalled 87 lots of losartan tablets USP 25mg, 50 mg and 100 mg. Legacy Pharmaceutical Packaging, LLC on March 15 recalled 43 lots of losartan tablets. Sandoz’s product was made using an active … "Americans expect their blood pressure medicadtion to treat their conditions, not cause cancer. Nearly 8 out of 10 active pharmaceutical ingredients, which are made into pills at other plants, are, too.This globalization of the nationâs drug supply helps keep prices down, as it is cheaper to have them made in other countries. Teva expanded this recall on June 10, 2019, with another six lots of losartan potassium USP tablets in 50mg and 100mg strength.  On May 4, Vivimed Life Sciences Pvt Ltd recalled 19 lots of losartan potassium tablets in 25 mg, 50 mg and 100 mg doses.
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