C.O. Truxton Expands Recall
The company is expanding their April 2017 voluntary recall of phenobarbital tablets.
On May 8, 2017, C.O. Truxton announced it was expanding its voluntary recall of phenobarbital tablets to all products repackaged with a Truxton Incorporated label out of caution. The original recall of phenobarbital tablets, issued April 21, 2017, was due to mislabeled product. The new recall extends to amitriptyline tablets, USP 52 mg.
An overdose of amitriptyline, which is used as a tricyclic antidepressant, could lead to uneven heartbeats, extreme drowsiness, confusion, agitation, vomiting, hallucinations, hot or cold sensations, muscle stiffness, seizures (convulsions), or fainting in humans. The company has not received any reports of adverse events associated with the recalled products as of May 8, 2017.
Source: FDA
Trump Directs FDA, EPA to Reduce Regulatory Barriers to Domestic Pharma Manufacturing
May 7th 2025The White House is instructing FDA to increase fees for and inspections of foreign drug manufacturing plants and reduce the time required to approve such sites that will be newly constructed in the US.
New Cancer Research and Treatment Center in Development in London
May 1st 2025Aviva Capital Partners and developer Socius are investing £1 billion in a 12-acre site to be located at the London Cancer Hub next to The Institute of Cancer Research, London and The Royal Marsden NHS Foundation Trust’s Sutton site.
