The company voluntarily initiated the recall after a batch of bottles containing 60 3-mg tablets of the drug failed dissolution specifications. An FDA report sent out Thursday reveals the recall affects tablets with expiration dates into 2027. National Library of Medicine data in 2019 … The voluntary recall of Xanax XR in the U.S. is specific to one lot of one strength (3mg) of the brand product only, and no other batches of the … The recalled bottles of Xanax were distributed nationwide between Aug. 27, 2024, and May 29, 2025, according to the California State Board of … The recall has been classified as a Class II, meaning the affected products could cause adverse reactions. Recalled Xanax pills: What to know. The recalled pills were distributed in 60-pill bottles between August 2024 and May 2025, according to Viatris. Bottles of the affected pills are … The FDA is investigating and recalling select bottles of Xanax after the pills failed to dissolve properly during testing. 3 mg Xanax XR tablets (60-count bottles) were first recalled on March 17, with the recall expanded nationwide on April 15 after the medication … So, why specifically is this lot being recalled? Well, the stated reason is “failed dissolution specifications.” That may sound like something … The recall, initiated on March 17, affects 3-milligram tablets packaged in 60-tablet bottles, produced in Ireland and distributed by Viatris … Lot number 8177156 was recalled, with bottles containing 60, 3mg extended-release tablets. The expiration date for the bottles was Feb. 28, 2027 … Xanax XR (alprazolam) extended release. 00009006807. Failed Dissolution … Aurobindo Pharma, 1-866-. 850-2876. February. 2022. Class II. The recall occurred because the pills failed dissolution specifications, the FDA said. The recalled Xanax came in 3 mg pills with the bottles … According to the notice, the drug was recalled because it \ »failed dissolution specifications.\ » This means the drug may have failed quality … A nationwide recall has been issued for a batch of Xanax XR after the manufacturer found the medication may not release as intended. Dr Reddy\’s Laboratories is recalling close to 20,000 cartons of a medication used to control blood phenylalanine levels in adults and children. Lot number 8177156 was recalled, and the bottles contained 60 3 mg extended-release pills. The expiration date for the impacted bottles is Feb. On March 17, the distributor recalled 3-milligram tablets of Xanax XR, sold in 60-tablet bottles. On April 15, the pills were recalled … ANI Pharmaceuticals Inc is recalling more than 500,000 bottles of alprazolam tablets because of deviations from Current Good Manufacturing … ANI Pharmaceuticals Inc is recalling more than 500,000 bottles of alprazolam tablets because of deviations from Current Good Manufacturing … Aurobindo Pharma USA, Inc. has initiated a voluntary recall of two (2) lots (refer table below) of Quinapril and Hydrochlorothiazide Tablets USP 20mg / 12.5mg, … Drug makers Aurobindo Pharma, Glenmark and FDC are recalling products in the US due to manufacturing issues, as per the US Food and Drug Administration (USFDA). The specific product included in the recall was: Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles, Rx only … The recall covers lot number 8177156 — 60-tablet bottles of 3mg extended-release tablets with an expiration date of Feb. 28, 2027. A Class II … 11/19/24 Endo USA, Inc. Clonazepam Orally Disintegrating Tablets, USP (C-IV) 60 count carton presentation. 11/18/24 Aurobindo Pharma USA, Inc. Xanax (alprazolam) pills are being voluntarily recalled by the American pharmaceutical company Viatris Inc. because the drug failed to meet … Most recently, there was a recall of Alprazolam, Mylan\’s generic version of the anti-anxiety medicine Xanax due to contamination from a foreign … The recall affects only one lot of 3 mg Xanax tablets provided in 60-tablet bottles, though the FDA has not indicated how many pills or bottles … The recall is for 3 mg Xanax XR, the brand name for alprazolam. Affected items are in 60 tablet bottles. The recall was voluntary and initiated …
