Which losartan was recalled

    • [PDF File]Recall of 3 brands of Losartan Medicines Frequently Asked ...

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      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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    • [PDF File]Drug Recall List

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      related to using the recalled losartan. • Anyone with an existing inventory of the recalled product should stop use and distribution, and quarantine the product immediately. • For more information regarding this recall, contact Camber Pharmaceuticals at 1-866-495-1995.

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    • [PDF File]Camber Pharmaceuticals – Recall of losartan

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      — Previously on December 20, 2018, Torrent had recalled several lots/NDCs of losartan tablets for the same reason. • NDEA is a substance that occurs naturally in certain foods, drinking water, air pollution, and industrial processes, and has been classified as a probable human carcinogen as per International

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    • [PDF File]Torrent – Recall of Losartan

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      Jan 15, 2019 · Losartan Recalled by Torrent Product Description NDC# Lot# (Expiration Date) Losartan 50 mg unit dose tablets 0904-6390-61 R-00474 (7/2019) Due to the large scale and ongoing nature of Angiotensin Receptor Blocker (ARB) recalls, certain ARB products, such as Valsartan, may be in limited supply for the near-term.

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    • [PDF File]Teva – Recall of losartan

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      related to using the recalled losartan/HCTZ. • Anyone with an existing inventory of the recalled product should stop use and distribution, and quarantine the product immediately. • For more information regarding this recall, contact Sandoz by phone at . 1-800-525-8747 or by email at usdrugsafety.operations@novartis.com.

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    • [PDF File]Torrent – Recall of losartan

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      • The bulk recalled lots were sold exclusively to Golden State Medical Supply. Golden State Medical Supply packaged these products under its own label and distributed retail bottles of 30, 90 and 1000 tablets. Product Description NDC# Lot# (Expiration Date) Losartan 50 mg tablets

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    • [PDF File]Losartan Recall - medSask

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      related to using the recalled losartan. • Anyone with an existing inventory of the recalled product should stop use and distribution, and quarantine the product immediately. • For more information regarding this recall, contact Torrent at 1-800-912-9561 or Qualanex at 1-888-280-2020 for general questions regarding return of the product.

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    • [PDF File]Recall of Losartan by Major

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      The Health Sciences Authority (HSA) has recalled three brands of high blood pressure medicine which contain losartan – Losartas, Losagen and Hyperten – on 28 March 2019. Seven other brands of losartan medicine approved in Singapore are not affected by the recall. 2. Why are three brands of high blood pressure medicines being recalled?

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    • Losartan Latest BP Drug Recalled for Contamination

      * Drug Recall Class Class 1 Recall: Reasonable probability that using the drug will cause serious adverse health consequences or death. 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.

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    • [PDF File]Sandoz – Recall of Losartan/Hydrochlorothiazide

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      Losartan Recall Due to the presence of a potentially carcinogenic contaminant: N-nitroso-N-methyl-4-aminobutyric acid (referred as “NMBA”), Health Canada has recalled Teva-Losartan / HCTZ 50/12.5mg.

      which losartan has been recalled 2019


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