News Reader
04-10-2009, 08:23 AM
The U.S Food and Drug Administration today amended its March 30, 2009, action warning manufacturers to stop the production and distribution of certain unapproved prescription opioids, to allow the continued marketing and distribution of one particular type of opioid -- a high concentrate morphine sulfate oral solution -- on an interim basis.
More... (http://www.fda.gov/bbs/topics/NEWS/2009/NEW01994.html)
More... (http://www.fda.gov/bbs/topics/NEWS/2009/NEW01994.html)