Fda list of recalled valsartan

• [PDF File]Recall Notice: Valsartan and Valsartan Combination ...

  https://info.5y1.org/fda-list-of-recalled-valsartan_1_9aafbc.html

  Recall Notice: Valsartan and Valsartan Combination Products are Recalled by FDA- Updates August 2018 The medication valsartan and the combination drugs valsartan-hydrochlorothiazide (valsartan-hctz) and valsartan-amlodipine-hydrochlorothiazide (amlodipine-valsartan-hctz) from certain manufacturers, have been recalled by the U.S. Food and Drug

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• [PDF File]FDA recalls

  https://info.5y1.org/fda-list-of-recalled-valsartan_1_5769d0.html

  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 searchable list maintained by the FDA . here.

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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 . U.S. Food & Drug Administration 10903 New Hampshire Avenue Silver Spring. MD 20993 FDA.GOV

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• [PDF File]Aurobindo Pharma – Recall of Valsartan- Containing Products

  https://info.5y1.org/fda-list-of-recalled-valsartan_1_1bdca7.html

  — Refer to the FDA site for updates regarding angiotensin II receptor blocker recalls. • The recalled products were distributed nationwide. Refer to the Aurobindo Pharma announcement for the list of specific recalled NDC numbers and lot numbers. • Valsartan is used tocontrol high blood pressure and for the treatment of heart failure.

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• [PDF File]Valsartan Recall – Update

  https://info.5y1.org/fda-list-of-recalled-valsartan_1_7323f2.html

  • The FDA reminds patients taking valsartan from a recalled lot to continue taking their current medicine until their doctor or pharmacist provides a replacement or a different treatment option. Any patient taking valsartan from a recalled lot who has not yet spoken to their pharmacist or doctor should do so promptly.

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• [PDF File]Diovan - Food and Drug Administration

  https://info.5y1.org/fda-list-of-recalled-valsartan_1_3ed13b.html

  Valsartan inhibits the pressor effect of angiotensin II infusions. An oral dose of 80 mg inhibits the pressor effect by about 80% at peak with approximately 30% inhibition persisting for 24 hours. No information on the effect of larger doses is available.

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• [PDF File]Camber and NuCare – Recall of Valsartan

  https://info.5y1.org/fda-list-of-recalled-valsartan_1_de7462.html

  Camber and NuCare – Recall of Valsartan • On August 9, 2018, the FDA announced an update to the list of valsartan products under recall and the list of valsartan products not under recall to incorporate recalls of valsartan-containing products manufactured by Hetero Labs Limited, in India, labeled as Camber Pharmaceuticals Inc.

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• valsartan products under recall

  Valsartan products under recall - Updated April 11, 2019. Page 2 of 10 Company Product NDC Package Code Lot Expiration Aurobindo Pharma USA, Inc. Amlodipine/Valsartan 10mg/160mg Tablet 65862-739-30 VFSA18002-A 01/2020 ... valsartan products under recall FDA ...

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• [PDF File]The United States: FDA updates on valsartan recalls

  https://info.5y1.org/fda-list-of-recalled-valsartan_1_623033.html

  The United States: FDA updates on valsartan recalls The US Food and Drug Administration (FDA) continues to evaluate valsartan-containing products and has updated the list of products included in the recall and the list of products not included in the recall on 2 Aug 2018. The agency will continue to provide information when it becomes available.

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• [PDF File]Drug Recall List

  https://info.5y1.org/fda-list-of-recalled-valsartan_1_f0a853.html

  NOTE: This is not a complete list of all recalls. Please see FDA.gov >Drugs>Drug Safety and Availability> Drug Recalls for additional information. Drug Recall List Last Updated: July 2019 . Drug Recall Details Contact Date Drug Recall Class* Milrinone lactate 00409277602, 00409277623

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