Aurobindo xanax recall

The company voluntarily initiated the recall after a batch of bottles containing 60 3-mg tablets of the drug failed dissolution specifications. 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, … The FDA classified this as a Class II recall, indicating the risk of serious harm is low, but temporary or reversible health effects are … If you have questions about this recall, call Aurobindo Pharma, 1-866- 850-2876. Xanax XR (alprazolam) extended release 00009006807 Failed … The FDA announced a voluntary recall of select lots of Xanax. · The impacted lots may dissolve too quickly or not fast enough in the body. Xanax XR (alprazolam) Extended-release Tablets 3mg, 60 tablet bottle. Aurobindo Pharma USA, Inc. Aurobindo Pharma USA, Inc. Alprazolam Tablets CIV 0.25mg, 0.5 … The recall, initiated on March 17, affects 3-milligram tablets packaged in 60-tablet bottles, produced in Ireland and distributed by Viatris … The FDA is investigating and recalling select bottles of Xanax after the pills failed to dissolve properly during testing. Xanax (alprazolam) pills are being voluntarily recalled by the American pharmaceutical company Viatris Inc. because the drug failed to meet … A widely used anti-anxiety drug has come under scrutiny after US regulators announced a voluntary recall of a specific batch of Xanax XR. AuroHealth is voluntarily recalling one lot (refer table below) of Healthy Living Migraine Relief, Acetaminophen 250mg, Aspirin (NSAID) 250mg & Caffeine 65mg … According to the FDA, the voluntary recall was listed as a \“Class II\“ recall, which means temporary, adverse health consequences are possible. 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 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 generic drug alprazolam is unstable, varies in effectiveness and sometimes doesn\’t seem to have any effect at all. A nationwide recall has been initiated for certain bottles of Xanax. The anti-anxiety medication failed quality testing that could impact … Dr Reddy\’s Laboratories is recalling close to 20,000 cartons of a medication used to control blood phenylalanine levels in adults and children. A nationwide recall has been issued for a batch of Xanax XR after the manufacturer found the medication may not release as intended. The U.S. Food and Drug Administration has listed a voluntary recall of a single lot of Xanax XR by a distributor of the medication, Viatris, … According to WKYT, 3 mg Xanax XR tablets (60-count bottles) were first recalled on March 17, with the recall expanded nationwide on April 15 … According to the notice, the drug was recalled because it \“failed dissolution specifications.\“ This means the drug may have failed quality … The 3-milligram tablets were sold 60 to a bottle under lot No. 8177156 and carry an expiration date of Feb. 28, 2027. The FDA\’s Class II recall … As for Aurobindo, the company recalled a total of 96 bottles of rufinamide tablets for treating seizure disorders. The company\’s recall covers … The affected medication includes three-milligram Xanax XR tablets sold in bottles of 60, labeled under lot number 8177156 with an expiration … 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, issued March 17, affects lot number 8177156. The bottles contain 60 tablets of the 3-milligram extended-release version of the … On March 17, the distributor recalled 3-milligram tablets of Xanax XR, sold in 60-tablet bottles. On April 15, the pills were recalled … 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 … Lot number 8177156 was recalled, and the bottles contained 60 3 mg extended-release pills. The expiration date for the impacted bottles is Feb.