Losartan recall list of manufacturers

• [PDF File]Torrent – Recall of losartan/hydrochlorothiazide

  https://info.5y1.org/losartan-recall-list-of-manufacturers_1_af0c27.html

  Torrent – Recall of losartan/hydrochlorothiazide • On January 22, 2019, Torrent announced an expansion of their voluntary, consumer-level recall of losartan tablets to include several lots of losartan/hydrochlorothiazide (HCTZ) tablets due to the detection of trace amounts of an unexpected impurity, identified as N-nitrosodiethylamine (NDEA),

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• [PDF File]PATIENT INFORMATION LOSARTAN POTASSIUM TABLETS …

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  PATIENT INFORMATION LOSARTAN POTASSIUM TABLETS USP 25 mg, 50 mg, 100 mg Rx only Read the Patient Information that comes with losartan potassium tablets before you start taking it and each time you get a refill. There may be new information. ... complete list …

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• [PDF File]Irebesartan products under recall

  https://info.5y1.org/losartan-recall-list-of-manufacturers_1_869585.html

  Page 1 of 1 Company Product NDC Package Code Lot Expiration Prinston Pharmaceutical Inc., dba Solco Healthcare LLC Irbesartan 300mg Tablet 43547-376-09 331B18009 02/2021

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• [PDF File]COZAAR® (LOSARTAN POTASSIUM TABLETS) Page 1 of 28

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  COZAAR® (LOSARTAN POTASSIUM TABLETS) Page 2 of 28 do not exhibit any partial agonist activity at the AT1 receptor and have much greater affinity (about 1000-fold) for the AT1 receptor than for the AT2 receptor.In vitro binding studies indicate that losartan is a reversible, competitive inhibitor of the AT1 receptor.The active metabolite is 10 to 40 times more potent by weight than

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• [PDF File]Recall of Losartan by Major - OptumRx

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  Jan 15, 2019 · Recall of Losartan by Major Effective Date: January 11, 2019 On January 11, 2019, Major announced a voluntary recall of one lot of unit dose Losartan tablets because of the presence of trace amounts of an unexpected impurity, N-nitrosodiethylamine (NDEA), found in the finished product. NDEA is classified as a probable human carcinogen.

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• [PDF File]Valsartan recall product supply shortage for Alberta Drug ...

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  Valsartan recall product supply shortage for Alberta Drug Benefit List (ADBL) On July 9, 2018, Health Canada issued an advisory for select valsartan products that have been recalled by the manufacturer. For listings of specific products included in the recall, please refer to the advisory issued by Health Canada, which can be found online at:

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• [PDF File]Drug Recall List

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  Class 2 Recall: Using the drug may cause temporary or medical reversible adverse health consequences, the probability of serious adverse health consequences is remote. Class 3 Recall: Using the drug is not likely to cause adverse health consequences. NOTE: This is not a complete list of all recalls.

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• FDA FACT SHEET

  FDA FACT SHEET. Find the list on the following webpage: Search List of Recalled Angiotensin II Receptor Blockers (ARBs) including Valsartan, Losartan and Irbesartan

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• Table 1 - List of Valsartan-containing parallel imported ...

  Table 1 - List of Valsartan-containing parallel imported products included in the recall of 11 July 2018. Please note that Diovan and Co-Diovan products marketed by Novartis are not affected by the impurity issue and are therefore not included in this recall action.

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• [PDF File]FDA recalls - OptumRx

  https://info.5y1.org/losartan-recall-list-of-manufacturers_1_5769d0.html

  a recall for losartan-containing products. The FDA has issued recalls for several medications in the angiotensin receptor blocker (ARB) category, including losartan-containing products and valsartan-containing products. These recalls involve multiple manufacturers. To check if your prescription contains a recalled medication, please see the

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