Lupin Pharmaceuticals Irbesartan Recall -

18/01/2019 · A drug company on Friday announced the recall of eight more lots of irbesartan blood pressure medication after testing revealed the drugs contained trace amounts of a carcinogen. Prinston Pharmaceuticals recalled one lot of irbesartan tablets and seven lots of irbesartan HCTZ tablets. The. The U.S. Food and Drug Administration FDA has announced the recall of popular blood pressure medication Irbesartan, after finding an impurity that could cause cancer, months after it recalled Valsartan over similar reasons. 20/01/2019 · PREVIOUS STORY: Company Expands Recall of Popular Blood-Pressure Drug Losartan; Solco Healthcare LLC recalled one lot of irbesartan 150 mg and 300 mg tablets, and seven lots of irbesartan and hydrochlorothiazide-combination 150 mg and 300 mg tablets. The FDA has already announced several recalls for irbesartan in the past few months.

31/10/2018 · Sciegen Pharmaceuticals, Inc. issues voluntary nationwide recall of Irbesartan tablets, USP 75 mg, 150 mg, and 300 mg due to the detection of trace amounts of NDEA N-nitrosodiethylamine impurity found in the active pharmaceutical ingredient. Published on: October 30, 2018. Accessed on: October 31, 2018. about this recall, Lupin Pharmaceuticals 1-800-399-2561 July 2019 Class II Milrinone lactate 00409277602, 00409277623 Bags have the potential to leak If you have questions about this recall, Pfizer Inc. 1-800-879-3477 July 2019 Class II Drug Recall Class Class 1. 04/01/2019 · A recall of Torrent Pharmaceuticals Limited ’ s Losartan Potassium Tablets USP has been expanded to include 8 additional lots. A total of 10 lots are now being recalled at the consumer level, including 2 recalled lots initially announced December 20, 2018.

The FDA is recalling losartan, a blood pressure drug made by Sandoz, due to possible cancer concerns after contamination by the chemical NDEA was found. One lot of losartan is contaminated with NDEA, an organic chemical used to make liquid rocket fuel and could cause cancer. Information about the prescription drugs manufactured by Lupin Pharmaceuticals, Inc.

/ Blood Pressure Meds Alert: Irbesartan Recall. Zhejiang Huahai Pharmaceuticals, was found to have produced tainted pills, so the FDA placed this company on an import alert in September 2018; all active pharmaceutical products made by this company are not permitted to enter into the United States. Lupin Pharmaceuticals, Inc. Issues Voluntary Recall of Ceftriaxone for Injection USP, 250mg, 500mg, 1g and 2g Lupin receives FDA approval for Lurasidone Hydrochloride Tablets, 20 mg, 40 mg, 60 mg, 80 mg & 120 mg Lupin receives FDA approval for Clobazam Oral Suspension, 2.5 mg/mL.

New Delhi: Lupin's US arm is recalling 11,706 bottles of Lisinopril tablets, used for treating hypertension, from the American market, USFDA said. The product being recalled by Lupin Pharmaceuticals Inc is in the strength of 10mg, the US health regulator said in an Enforcement Report.

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