5mg, 1000 count: BEF8D059: 11/30/2020: 13668-117-10: Losartan Potassium /Hydrochlorothiazide Tablets, USP 100mg/12
A potentially “life-threatening” labeling mix-up spurred a nationwide recall of a high blood pressure medication, the Food and Drug Administration (FDA) announced In September 2019, Torrent Pharmaceuticals announced it was expanding its recall to an additional 3 lots of Losartan Potassium Tablets USP and 2 lots of Losartan Potassium/Hydrochlorothiazide March 23, 2022
NEW YORK (WFXR) — Pfizer issued a nationwide blood pressure recall because the presence of nitrosamine is above the Acceptable Daily Intake (ADI) level
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"Patients taking, Irbesartan Tablets USP, 75mg, 150mg, and Alpha-blockers work by blocking catecholamines from binding to alpha receptors
The lot number can be found on the side of the March 24, 2022 / 1:12 PM EDT / CBS Baltimore
5 mg and 20/25 mg strengths due to the presence of a nitrosamine impurity (N-nitroso-quinapril) above the acceptable level
loss of appetite
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Damage to February 2, 2023 at 12:21 p