The voluntary recall began with two lots of Losartan potassium tablets USP on Jan. 3 before being expanded. The recall of Torrent's Losartan products was initially announced December 20, 2018, and was expanded on January 3, 2019. Kopalle Pharma Chemicals Pvt Ltd is an ISO 9001:2015 Certified Company and has a GMP Certified manufacturing facility at Jeedimetla, Hyderabad. The company said in the statement that for this recall "it has not received any reports of … 3801. These type of medications work by preventing the constriction (narrowing) of blood vessels (veins and arteries). Camber Pharmaceuticals on Feb. 28 recalled 87 lots of losartan tablets USP 25mg, 50 mg and 100 mg. See the affected products and what the label looks like. IMPORTANT: Continue Taking Your Meds. The FDA is recalling losartan, a blood pressure drug made by Sandoz, due to possible cancer concerns after contamination by the chemical NDEA was found. (4)Common side effects of Losartan potassium can include: (4)If you’re interested in learning more about effective ways to help manage high blood … According to the FDA, the recalled medications contain an ingredient made by Hetero Labs in India, one of three overseas factories linked to recalls of drugs commonly prescribed for high blood pressure since July. Omnia Sports - C.F./P.Iva: 04258560616. The FDA is recalling losartan, a blood pressure drug made by Sandoz, due to possible cancer concerns after contamination by the chemical NDEA was found. Locally, Losartan and valsartan are two of the biggest selling hypertension medications, say pharmacists, who also say they’ve been inundated with calls since the recalls began. TAB, USP. manufacturers and suppliers of losartan from around the world. Panjiva uses over 30 international data sources to help you find qualified vendors of losartan. E 'probabilmente qualche cosa che abbiamo fatto di sbagliato, ma ora sappiamo su di esso e cercheremo di risolvere il problema. Torrent Pharmaceuticals voluntarily recalled two lots of losartan potassium tablets because of trace amounts of an impurity that has been found … In September 2018, the FDA announced it had found another toxic chemical in tainted valsartan batches called N-nitrosodiethylamine (NDEA). The United States Food and Drug Administration (FDA) approved the drug Losartan potassium in 1995 to treat hypertension. NDC Manufacturer Product Description Lot/Batch Exp. The drugs were made in India and distributed by … According to the FDA, the product can be identified by checking the product name, manufacturer details and batch or lot number on the bottle containing these products. Skip to main … The FDA has traced the recalled drugs to Chinese manufacturers Zhejiang Huahais and Zhejiang Tianyu as well as Hetero Labs Limited in India. STREAMBASKET All 3 medicines contain losartan, an angiotensin II receptor blocker (ARB) commonly uused to treat hypertension. The voluntary recall began with two lots of Losartan potassium tablets USP on Jan. 3 before being expanded. Recall Expanded for Losartan Potassium Tablets. The losartan API, produced by the first company embroiled in the recall – Zhejiang Huahai Pharmaceuticals – was also found to contain NDEA. Macleods also recalled one lot of the losartan combination drug in February for the same reason. On January 3, 2019, the manufacturer (Torrent Pharmaceuticals Limited) of losartan potassium tablets recalled certain lots of the product. Losartan Recalled Due to Traces of a Hazardous Carcinogen Dangerous Drugs Macleods Pharmaceuticals Limited, the manufacturers of the blood pressure drug Losartan, has announced that they will begin recalling their product after trace amounts of the carcinogen N-nitrosodiethylamine—otherwise known as NDEA—were detected. Alibaba offers 158 Losartan Suppliers, and Losartan Manufacturers, Distributors, Factories, Companies. Pills made by the India-based pharmaceutical manufacturer Torrent have been “voluntarily recalled” because of cancer risk. Tell us whether you accept cookies. Losartan Potassium. The losartan API was manufactured by Zhejiang Huahai Pharmaceutical. It may be used alone or in combination with other agents. Only one lot was recalled – Losartan Potassium Hydrochlorothiazide Tablets by Sandoz Inc. Pertanto A.S.D. According to the FDA, NDEA occurs naturally in certain foods, drinking water, air pollution and industrial processes, and has been classified as a probable human carcinogen. Losartan Potassium Tablet and Losartan Potassium / Hydrochlorothiazide Tablet Lots-Advertisement-NDC Product Name, Strength and Package Count Batch Number Expiration Date; 13668-409-10: Losartan … The product can be identified by checking the product name, manufacturer details and batch or lot number on the bottle containing these products. Losartan is used to treat hypertension, hypertensive patients with Left Ventricular Hypertrophy and nephropathy in type 2 diabetic patients. A maker of losartan potassium is recalling this medicine because they may have small amounts of an ingredient which could cause cancer. Apotex has issued a voluntary recall of several lots of generic blood pressure medications enalapril / hydrochlorothiazide (enalapril/HCTZ, generic Vaseretic) and losartan (generic Cozaar). Founded in 2017 by a team with vast experience across the pharmaceutical value chain, the company is on a mission to become the most preferred partner for pharmaceuticals. This page was last updated: 3/20/19. They include Aurobindo Pharma USA, which recently recalled 80 lots of valsartan tablets. The recalled losartan potassium and losartan potassium/hydrochlorothiazide tablets are also manufactured by Hetero, which are distributed by Camber, and contain the impurity NMBA. Losartan and losartan potassium are the same medication and belong to a class of drugs called angiotensin II receptor blockers (ARBs). Teva has recalled other valsartan-containing products in recent months due to the presence of N-Nitrosodimethylamine (NDMA). On May 4, Vivimed Life Sciences Pvt Ltd recalled 19 lots of losartan potassium tablets in 25 mg, 50 mg and 100 mg doses. Patients should contact their pharmacist or physician about alternative treatments prior to returning the medication. Losartan Potassium Tablets, USP were distributed nationwide, according to the FDA. In this case, the manufacturer has voluntarily recalled one lot of enalapril/HCTZ 10 mg/25 mg tablets, and four lots of losartan 25 mg, 50 mg, and 100 mg tablets. With the recall of yet another blood pressure medication called losartan announced last month by the U.S. Food and Drug Administration, the safe supply of some generics is a real concern. The FDA advises patients on Losartan to continue taking their medication, as the risk of harm to the patient’s health may be higher if treatment is stopped immediately. Hi I have been taking this medication LOSARTAN since 2007 then I notice that it started making me really sick , bad cough noe I have a cyst on my kidney. KU To Shut Down E.W. Macleods … Direttore responsabile: Umberto De Maria. Authorities found ingredients made by Hetero Labs and Zhejiang Huahai Pharmaceutical Company and Zhejiang Tianyu Pharmaceuticals, both of China, contained a known carcinogen. To the FDA said recent months due to the FDA said ( narrowing ) Singapore. 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