Fda losartan potassium recall 2019

• [PDF File]Losartan Potassium tablets May 3, 2019 acid (NMBA) Impurity

  https://info.5y1.org/fda-losartan-potassium-recall-2019_1_f068ee.html

  Drug recall notice for Losartan Potassium tablets May 3, 2019 Vivimed Life Sciences Pvt Ltd Issues Voluntary Nationwide Recall of Losartan Potassium 25 mg, 50 mg and 100 mg Tablets, USP Due to the Detection of Trace Amounts of N-Nitroso-N-methyl-4-aminobutyric

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• [PDF File]Updated: Torrent Pharmaceuticals Limited Expands Voluntary ...

  https://info.5y1.org/fda-losartan-potassium-recall-2019_1_e5c660.html

  Sep 23, 2019 · Losartan Potassium Tablets, USP and Losartan Potassium / Hydrochlorothiazide Tablets, USP September 23, 2019 Torrent Pharmaceuticals Limited is expanding its recall for Losartan Potassium Tablets USP and Losartan Potassium/hydrochlorothiazide tablets, USP, to the consumer level due to the detection of trace amounts of an

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• Development and validation of a RapidFire-MS/MS method …

  Losartan potassium is used to treat high blood pressure. From November 2018 to March 2019, FDA alerted patients and health care professionals to the recall of losartan potassium

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• [PDF File]Drug Information Center Highlights of FDA Activities – 6/1 ...

  https://info.5y1.org/fda-losartan-potassium-recall-2019_1_a296d9.html

  FDA Activity Newsletter WSU Drug Information June 2019 Drug Information Center ... Losartan Potassium 50 mg and 100 mg Tablets USP, from Teva Pharmaceuticals USA, Inc. ... 6/11/19 This expanded recall includes 6 lots of bulk losartan potassium USP Tablets (two …

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• [PDF File]Drug recall notice for Losartan Potassium and Losartan ...

  https://info.5y1.org/fda-losartan-potassium-recall-2019_1_d4208d.html

  Drug recall notice for Losartan Potassium and Losartan Potassium Hydrochlorothiazide tablets May 3, 2019 Updated: Torrent Pharmaceuticals Limited Expands Voluntary Nationwide Recall of Losartan Potassium Tablets, USP and Losartan Potassium/Hydrochlorothiazide Tablets, USP ... intake levels released by the FDA.

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• Losartan products under recall - Updated March 19, 2019 ...

  Losartan Potassium 50mg Tablets, 50-count bottle 50268-517-15 20961 20477 Sep-19 ... Losartan products under recall - Updated March 19, 2019. Camber Pharmaceuticals, Inc. Page 1 of 10.

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• [PDF File]Recall of Losartan by Legacy Effective Date: April 24, 2019

  https://info.5y1.org/fda-losartan-potassium-recall-2019_1_ede6db.html

  FDA Safety Alert. Legacy Pharmaceutical Packaging, LLC Expands Voluntary Nationwide Recall of Losartan Potassium Tablets, USP, 50mg Due to the Detection of Trace Amounts of N-Nitroso N-Methyl 4-amino butyric acid ... 2019. 2. FDA Safety Alert. FDA updates on angiotensin II receptor blocker (ARB) recalls including valsartan, losartan and ...

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• [PDF File]Drug Recall List - Blue Cross Blue Shield of Michigan

  https://info.5y1.org/fda-losartan-potassium-recall-2019_1_f0a853.html

  Class 3 Recall: Using the drug is not likely to cause adverse health consequences. NOTE: This is not a complete list of all recalls. Please see FDA.gov >Drugs>Drug Safety and Availability> Drug Recalls for additional information. 00597012261 00597012281, 00597012296 Regular Strength Zantac® 05026922225, 06775115101, 06775115201, 06775115202,

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• [PDF File]Drug Recall - AllWays Health Partners

  https://info.5y1.org/fda-losartan-potassium-recall-2019_1_c9df14.html

  10/2019 Losartan potassium 50mg tablets 1,000 count bottles 13668-0409-10 4O50C005 11/2019 Losartan potassium 25mg tablets 90 count bottles 13668-0113-90 4O49C013 09/2019 Losartan potassium 100mg tablets 30 count bottles 13668-0115-30 BO31C016 04/2019 Losartan potassium 100mg tablets 90 count bottles 13668-0115-90 BO31C016 04/2019 Losartan ...

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• [PDF File]Drug Recall - AllWays Health Partners

  https://info.5y1.org/fda-losartan-potassium-recall-2019_1_00ea96.html

  May 03, 2019 · Drug Recall DATE OF RECALL: May 3, 2019 DRUG NAME: Losartan Potassium RECALLING FIRM: Vivimed Life Sciences Pvt Ltd REASON FOR RECALL: This recall was issued due to the detection of an impurity – N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) – that is above the US Food & Drug Administration’s interim acceptable exposure limit of 9.82 ppm.

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