A specific lot of the widely prescribed anti-anxiety drug Xanax has been recalled nationwide for not passing quality control tests according to the Food and Drug Administration.
A batch of the popular anti-anxiety medication Xanax has been recalled because it may not properly dissolve in the body, according to the U.S. Food and Drug Administration enforcement report. Viatris, ...
The FDA has confirmed a nationwide Class II recall of a specific lot of Xanax XR (alprazolam extended-release) after it failed dissolution tests, raising concerns about dosage consistency and ...
Viatris, which Pfizer created in 2020, voluntarily withdrew extended-release products made at a plant in Ireland after an ...
The FDA issued a voluntary recall of Xanax XR manufactured by Viatris due to failure to meet dissolution specifications, ...
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