Viatris, which Pfizer created in 2020, voluntarily withdrew extended-release products made at a plant in Ireland after an ...
Demonstration batch production achieves all prespecified test specifications for dissolution, content uniformity, blend ...
In 2019, Fisher Price recalled its rock and place sleeper after more than 30 infant deaths since its 2009 release. *** House ...
Connecticut Attorney General William Tong's office has said that it expects the state to receive as much as $64 million from ...
A new device analyzes pill dissolution rates to generate digital fingerprints that distinguish real from counterfeit drugs.
The Commissionerate of Food Safety and Drug Control, Rajasthan has issued a public alert after laboratory testing identified ...
The FDA issued a voluntary recall of Xanax XR manufactured by Viatris due to failure to meet dissolution specifications, ...
A widely prescribed medication for treating anxiety and panic disorders is being recalled nationwide, according to the FDA.
CT Insider on MSN
Anxiety medication Xanax recalled nationwide, according to FDA
The anxiety medication is being recalled due to "failed dissolution specifications." ...
In a fresh drug safety alert underscoring continued regulatory vigilance, 48 batches of drugs, medical devices, and allied ...
A specific lot of extended-release Xanax (alprazolam) tablets are being voluntarily recalled by the American pharmaceutical company Viatris Inc.
Viatris Specialty LLC initiated a nationwide retail-level recall of Xanax XR extended-release tablets, the company said in a notice to California’s Board of Pharmacy. The FDA classified the recall as ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results