Losartan recall 2019 fda list
[PDF File]Torrent Pharmaceuticals Limited Issues Voluntary Nationwide …
https://info.5y1.org/losartan-recall-2019-fda-list_1_2b7374.html
To view a full list of the products subject to recall click the following link . FDA Link. Losartan potassium tablets, USP and Losartan potassium/ hydrochlorothiazide tablets, USP were distributed nationwide to Torrent’s wholesale distributor, repackager and retail customers. Torrent Pharmaceuticals Limited
[PDF File]Drug Information Center Highlights of FDA Activities – 6/1/19 – …
https://info.5y1.org/losartan-recall-2019-fda-list_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. Repackaged by Golden State Medical Supply, Inc.: Recall – Impurity 6/11/19 This expanded recall includes 6 lots of bulk losartan potassium USP Tablets (two lots of 50 mg strength and four lots of 100 mg strength) due to the …
[PDF File]Recall of Losartan by Legacy Effective Date: April 24, 2019
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Recall of Losartan by Legacy Effective Date: April 24, 2019 On April 24, 2019, Legacy announced an expansion to the voluntary recall of some lots of Losartan tablets because of the presence of trace amounts of an unexpected impurity, n-nitroso n-methyl 4-amino butyric acid (NMBA) a possible process impurity or contaminant in an active pharmaceutical ingredient, manufactured by Hetero Labs. This is …
[PDF File]FDA recalls
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FDA recalls . On September 19, 2019, Torrent Pharmaceuticals issued. a recall for losartan-containing products. The FDA has issued recalls for several medications in the angiotensin receptor
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
[PDF File]Torrent – Recall of losartan/hydrochlorothiazide
https://info.5y1.org/losartan-recall-2019-fda-list_1_af0c27.html
— Torrent initially announced a consumer-level recall of losartan on December 20, 2018. The recall was then expanded on January 3, 2019 to include additional lots of losartan. • NDEA is a substance that occurs naturally in certain foods, drinking water, air pollution, and
[PDF File]Drug Recall List
https://info.5y1.org/losartan-recall-2019-fda-list_1_f0a853.html
2019 : Class II Amitiza® 64764008060, 64764024010, 64764024060 . 24 mcg capsules were found in a 8 mcg If you have questions about this recall, Mallinckrodt Pharmaceuticals 1314- - 654-2000 May 2019 : Class II Losartan Potassium tablets Presence of an impurity If you have questions about this recall, Golden May 2019 Class II
[PDF File]Torrent – Recall of losartan
https://info.5y1.org/losartan-recall-2019-fda-list_1_534802.html
Torrent – Recall of losartan • On January 3, 2019, Torrent announced a voluntary, consumer-level recall of some lots of losartan tablets due to the detection of trace amounts of an unexpected impurity, identified as N-nitrosodiethylamine (NDEA), found in an active pharmaceutical ingredient (API) manufactured by Hetero Labs.
Drug recall notice for losartan and losartan-containing drug products
Drug recall notice for losartan and losartan-containing drug products . The U.S. Food and Drug Administration (FDA) has issued recalls for losartan tablets due to an impurity in the manufacturing of these medicines. The FDA continues to monitor drugs in the angiotensin II
[PDF File]Irebesartan products under recall
https://info.5y1.org/losartan-recall-2019-fda-list_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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