Viatris, which Pfizer created in 2020, voluntarily withdrew extended-release products made at a plant in Ireland after an ...
The US Food and Drug Administration (FDA) on Wednesday released final guidance for sponsors on when a standard release test and criteria may be used in lieu of extensive method development and ...
The FDA issued a voluntary recall of Xanax XR manufactured by Viatris due to failure to meet dissolution specifications, ...
A specific lot of the widely prescribed anti-anxiety drug Xanax has been recalled nationwide for not passing quality control ...
Light Wave Reports on MSN
Xanax recalled nationwide over failed dissolution testing
If you have a bottle of Xanax XR at home, it is worth checking the lot number. The FDA has issued a nationwide recall of a ...
Teva is voluntarily recalling a single lot of Anagrelide Capsules, USP 0.5mg, due to dissolution failure that was detected during a routine stability test. Teva is voluntarily recalling a single lot ...
The Mirror US on MSN
Over 140,000 bottles of popular cholesterol drug recalled as drugs fail lab testing
The Food and Drug Administration (FDA) said in an enforcement report that several bottle sizes of Atorvastatin Calcium Tablets, 10-mg (Prescription Only) are impacted by the recall ...
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