The FDA has announced a nationwide Class II recall of over 4,000 bottles of pantoprazole sodium tablets after reports of ...
The recall of the prescription-only anxiety medication was initiated by its distributor, Viatris, on March 17 ...
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FDA issues Class II recall for pantoprazole tablets
The FDA has announced a Class II recall of certain 40mg pantoprazole sodium tablets after reports of unusual discoloration. The affected batch, produced by Hetero Labs and sold by Camber ...
If you take the prescription drug Xanax, you might want to consult your doctor before continuing to take it. A, Viatris, the manufacturer of Xanax, recalled 3-milligram extended-release tablets of ...
One batch of pantoprazole, a common heartburn or acid reflux medication, has been recalled due to tablet discoloration.
A batch of Xanax XR has been recalled nationwide after the manufacturer found the drug may not release properly in the body. The FDA classified the issue as moderate risk.
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, Inc. Here's what this means.
A nationwide recall has been issued for one specific lot (#8177156) of Xanax XR (alprazolam extended-release 3 mg) due to failing dissolution standards. The FDA classified the recall as Class II, ...
The FDA issued a voluntary recall of Xanax XR manufactured by Viatris due to failure to meet dissolution specifications, ...
Maybe you know someone who’s taken over-the-counter water pills casually, hoping to reduce some bloating before vacation or a ...
WASHINGTON, D.C. — A nationwide recall has been issued for a specific lot of Xanax XR, a commonly prescribed anxiety medication, after federal regulators and the drug’s manufacturer flagged a ...
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