Xanax sourced to West Virginia-based company recalled nationwide. What you need to know
A specific portion of the drug Xanax, which is often prescribed to treat mental health problems including anxiety and panic disorders, has been recalled due to the product’s potential to cause adverse health effects.
US Food and Drug Administration officials Announces voluntary recall of Xanaxalso known as alprazolam, It is distributed by West Virginia-based distributor Viatris Specialty LLC.
The distributor’s parent company, Viatris Inc., did not respond to The Times’ request for comment.
Xanax is one of the drugs most commonly prescribed by doctors to treat general anxiety and panic disorders, but addiction experts say it is considered a highly addictive substance, given its psychodynamic properties, which include creating feelings of euphoria. National Library of Medicine.
The medication is generally safe and beneficial when used as directed; Its intended effect lasts up to six hours. American Addiction Centers.
Viatris Private LLC. The FDA initiated a voluntary recall of the product late last month, according to officials. No illnesses or injuries were reported in connection with the withdrawn pills.
Why was this particular allocation of Xanax recalled?
Xanax tablets were included in the class II recall because the product did not meet dissolution specifications. dissolves at a standard speed.
The classification of Xanax tablets means that use or exposure to the product may cause temporary or medically reversible adverse health consequences. According to FDA.
Details of recalled prescription pills
The recalled product, Xanax XR, is extended-release tablets.
The tablets are 3 milligrams and there are 60 pills in a bottle.
The product’s code information is “Lot #8177156” and its expiration date is February 28, 2027. This information can be found on the pill bottle.
Where the product is sold
Xanax tablets were sold nationwide.
What should you do if you have a bottle of recalled Xanax?
When a prescription drug is subject to a class II recall, it is typically removed from shelves in retail stores, but patients and consumers can continue using the drug unless otherwise directed by the FDA or the recall company, officials said.
Neither the FDA nor Viatris has provided further information on whether consumption of Xanax pills will be stopped.
FDA officials say if you have questions or concerns about the recalled product, consult your doctor or pharmacist.
“In some cases, stopping your medication may be more harmful to your health than continuing to take the withdrawn medication,” the FDA said.
