Losartan recall 2019

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

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

  Losartan products under recall - Updated February 22, 2019 Losartan Potassium 100mg Tablets, 1000 count bottle 13668-115-10 13668-409-90 Losartan Potassium 50mg Tablets, 90 count bottle Losartan Potassium and Hydrochlorothiazide (HCTZ) 100mg/12.5mg Tablets, 90 count bottle 13668-117-90

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• See more news about Losartan Recall 2019 Filetype:Pdf

  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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• News about Losartan Recall 2019 Filetype:Pdf

  Drug Recall List Last Updated: July 2019 . Drug Recall Details Contact Date Drug Recall Class* Milrinone lactate 00409277602, 00409277623 . Bags have the potential to leak If you have questions ... 2019 : Class II Losartan Potassium tablets Presence of an impurity If you have questions about this recall, Golden May 2019 Class II * Drug Recall ...

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• [PDF File]Teva – Recall of losartan

  https://info.5y1.org/losartan-recall-2019_1_5a2d75.html

  On May 3, 2019, the U.S. Food and Drug Administration (FDA) announced a drug recall. The recall is voluntary. It is for specific lots of Losartan and Losartan Hydrochlorothiazide tablets1. The FDA issued the recall because the product may have a safety concern. Please call your pharmacy to find out if your drug could be part of this recall.

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• FDA FACT SHEET

  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. As a precaution, Teva, Apotex, Pharmascience, and Pro-Doc have voluntarily recalled other losartan products. For details

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• [PDF File]Drug Recall List

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

  Camber Pharmaceuticals – Recall of losartan • On February 28, 2019, the FDA announced the voluntary, consumer-level recall of several lots of Camber Pharmaceuticals’ losartan tablets due to the detection of trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA), a possible process impurity or contaminant in an active ...

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• [PDF File]IMPORTANT LOSARTAN AND LOSARTAN …

  https://info.5y1.org/losartan-recall-2019_1_3806c7.html

  Mar 18, 2019 · Drug Recall DATE OF RECALL: March 18, 2019 April 25, 2019 (additional lots included) DRUG NAME: Losartan Potassium RECALLING FIRM: Torrent Pharmaceuticals LTD REASON FOR RECALL: This recall was issued due to the detection an unexpected impurity found in an active pharmaceutical ingredient (API) manufactured by Hetero Labs Limited. The

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• [PDF File]Losartan Recall

  https://info.5y1.org/losartan-recall-2019_1_505ed3.html

  — This recall is an expansion to Teva’s recall of losartan that was originally initiated on April 25, 2019. • The source of the NMBA impurity was detected in one lot of active pharmaceutical ingredient, manufactured by Hetero Labs Limited, which was used in the manufacturing of …

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• [PDF File]Camber Pharmaceuticals – Recall of losartan

  https://info.5y1.org/losartan-recall-2019_1_b4a76c.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]Irebesartan products under recall

  https://info.5y1.org/losartan-recall-2019_1_869585.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

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