Telmisartan being recalled curently

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  • March 30, 2021 Alembic Pharmaceuticals is recalling 1 lot of Telmisartan Tablets 20mg due to a complaint related to incorrect product strength on the label

    Unspecified problems with blister packaging have prompted Glenmark Pharmaceuticals Inc to recall numerous lots of telmisartan and hydrochlorothiazide tablets, according to the August 17, 2022, US Food and Drug

    The recalled lot is listed below: T he following information was provided by Pfizer and the FDA

    Telmisartan tablet, Solco Healthcare US, 20 mg, bottle, 30 count, NDC 43541-0283-03; Telmisartan tablet, Solco Healthcare US, 40 mg, bottle, 30 count, NDC 43541-0284-03 Generic name: telmisartan [ TEL-mi-SAR-tan ] Brand name: Micardis

    Add Info Legal Issues There is currently no legal information available for this drug

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    62332-087-30

    Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems

    A Food and Drug Administration recall of a heart medication due to a cancer-causing chemical now includes two blood pressure medications

    Both are used to The recalled Telmisartan tablets have a lot number of 1905005661 and an NDC number of 62332-087-30

    Food and Drug Administration (FDA) announced yet another blood pressure medicine recall for contaminants that may cause cancer, a The United States: Alembic Pharmaceuticals Limited issues voluntary nationwide recall of Telmisartan Tablets, USP, 20 mg due to label mix-up The US Food and Drug Administration (FDA) announces that Alembic Pharmaceuticals, Inc is voluntarily recalling one lot of Telmisartan Tablets, USP, 20 mg, packaged in 30-count bottles, Lot

    The FDA found that more than a dozen manufacturers produced prescription

    Patients with depletion of intravascular volume should have the condition corrected or telmisartan tablets should be initiated under close medical supervision (see WARNINGS, Hypotension in Volume Depleted Patients)

    Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg, 30 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd

    21 March 2019

    Health Canada is publishing a complete list of angiotensin II receptor blocker (ARB) products recalled in Canada due to the presence of or the potential for nitrosamine impurities

    by calling toll-free at 1-855-568-2511, or by email at cs@auropharma

    Blood pressure response is dose-related over the range of 20 to 80 mg [see Clinical Studies (14

    Telmisartan Tablets, USP are available containing 20 mg, 40 mg or 80 mg of telmisartan, USP

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