The Department of Justice today announced the finalization
of an April proposal to improve the Drug Enforcement Administration’s ability
to control the diversion of dangerous drugs in the midst of the national opioid
crisis. Announced in April by Attorney General Jeff Sessions, the final rule
sent for publication today in the Federal Register establishes that DEA will
take into consideration the extent that a drug is diverted for abuse when it
sets its annual opioid production limits.
If DEA believes that that a particular opioid or a
particular company’s opioids are being diverted for misuse, this allows DEA to
reduce the amount that can be produced in a given year. These revised limits
will encourage vigilance on the part of opioid manufacturers, help DEA respond to
the changing drug threat environment, and protect the American people from
potentially addictive drugs while ensuring that the country has enough opioids
for genuine medical, scientific, research and industrial needs.
"The opioid epidemic that we are facing today is the
worst drug crisis in American history," Attorney General Sessions said.
"To help end it, DEA must make sure that we prevent diversion and abuse of
prescription opioids. Today's new rule, by taking diversion of these opioids
into account, will allow the DEA to be more responsive to the facts on the
ground. More importantly, it will help us stop and even prevent diversion from
taking place. The American people can be confident that we are now better
equipped to protect them from dangerous drugs and that this rule brings us one
step closer to finally ending this unprecedented crisis."
“These common-sense actions directly respond to the national
opioid epidemic by allowing DEA to use drug diversion as a basis to evaluate
whether a drug’s production should be reduced,” said DEA Acting Administrator
Uttam Dhillon. “This also opens the door for increased communication and better
information sharing between DEA and individual states, as we work together to
address the opioid problem plaguing our country.”
The final rule enhances the roles for the state attorneys
general. It requires DEA to share notices of proposed aggregate production
quotas, and final aggregate production quota orders, to the state attorneys
general. It also allows for a hearing if necessary to resolve an issue of
material fact raised by a state’s objection to a proposed aggregate production
quota as excessive in relation to legitimate U.S. need.
DEA also announced that the final rule allows DEA to
consider relevant information from the Department of Health and Human Services,
Food and Drug Administration, the Centers for Disease Control, and the Centers
for Medicare and Medicaid Services, as well as relevant information from the
states.
Following April’s announcement of the proposed rule changes,
DEA received more than 1,600 public comments in response.
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