List of recalled losartan tablets: free download. On-line document store on 5y1.org

[PDF File]Drug Information Center Highlights of FDA Activities – 4/1 ...
https://info.5y1.org/list-of-recalled-losartan-tablets_1_9ed992.html
Potassium/Hydrochlorothiazide Tablets, USP. A complete list of recalled lots can be found on the FDA website. A complete list of all recalled losartan products can also be found on the FDA website. The FDA continues to update the ARB recall information page.

Search List of Recalled ARBs: Valsartan, Losartan and ...
Search List of Recalled Angiotensin II Receptor Blockers (ARBs) including Valsartan, Losartan and Irbesartan. Find out which specific blood pressure medications are affected by the recall

[PDF File]Recall of Losartan by Legacy Effective Date: April 24, 2019
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Losartan Tablets Recalled by Legacy Pharmaceutical Packaging Product Description NDC # Lot # (Expiration Date) Losartan 50 mg 68645-494-54 181598 (2/2021)* *Additional lot recalled by Legacy. Refer to the FDA reference for a complete list of Losartan-Containing products recalled by Legacy.

[PDF File]Torrent Pharmaceuticals Limited Issues Voluntary ...
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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

Drug recall notice for losartan and losartan-containing ...
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]URGENT DRUG RECALL NIFEdipine 10 mg Capsules, USP
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URGENT DRUG RECALL NIFEdipine 10 mg Capsules, USP October 6, 2016 Page 1 of 1 Dear Valued Customer: This is to advise you of a voluntary recall of 1-lot of NIFEdipine 10 mg Capsules, USP. Specific product information are given in the sections that follow, which details (1) recalled product information, (2) reason for recall, (3) depth of recall,

Table 1 - List of Valsartan-containing parallel imported ...
Table 1 - List of Valsartan-containing parallel imported products included in the recall of 11 July 2018. Please note that Diovan and Co-Diovan products marketed by Novartis are not affected by the impurity issue and are therefore not included in this recall action.

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
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Torrent – Recall of losartan/hydrochlorothiazide • On January 22, 2019, Torrent announced an expansion of their voluntary, consumer-level recall of losartan tablets to include several lots of losartan/hydrochlorothiazide (HCTZ) tablets due to the detection of trace amounts of an unexpected impurity, identified as N-nitrosodiethylamine (NDEA),

[PDF File]Drug Recall List
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Losartan Potassium tablets Presence of an impurity If you have questions about this recall, Golden May 2019 Class II * Drug Recall Class . Class 1 Recall: Reasonable probability that using the drug will cause serious adverse health consequences or death. Class 2 Recall:

List of recalled losartan tablets