How to check if your anxiety medication is – Business News
Bottles of Xanax – one of probably the most widely-prescribed drugs for anxiety – have been recalled after failing a quality-control check, in accordance to the Food and Drug Administration.
Viatris, Inc., a Pennsylvania-based pharmaceutical firm, in March initiated a voluntary recall of its 60-tablet bottles of Xanax, citing “failed dissolution specifications,” food security regulators mentioned.
That means a drug has failed a high quality control check, implying the Xanax doesn’t ship the proper dosage over time and is not being correctly absorbed.
Bottles of Xanax have been recalled after failing a high quality control check, in accordance to the Food and Drug Administration. Soni’s – stock.adobe.com
Last week, the FDA categorised it as a Class II recall, that means use of the product could trigger “temporary or medically reversible adverse health consequences.”
The recalled bottles of Xanax had been distributed nationwide between Aug. 27, 2024, and May 29, 2025, in accordance to the California State Board of Pharmacy.
Patients ought to check their bottles for lot #8177156 and an expiration date of Feb. 28, 2027, to see if their prescriptions are included within the recall.
The California State Board mentioned the recall was made “out of an abundance of caution,” including it is not conscious of any experiences of hostile reactions.
The recalled bottles of Xanax had been distributed nationwide. desertsands – stock.adobe.com
Xanax is a benzodiazepine, or sedative, usually used to deal with panic and anxiety issues over a short-term foundation.
Viatris didn’t instantly reply to The Post’s request for remark.
