Douglas Throckmorton, deputy director for regulatory programs at the Food and Drug Administration, revealed the news during a lightly attended congressional hearing last week.
"Yes, I heard that," said Kyle Romanoff, a Washington, D.C.-based pharmaceuticals lobbyist. "Word is just beginning to get out."
Romanoff told Sunshine State News late Wednesday, "It will take a little while for the FDA to get around to it. Remember, you're talking about the federal government here. I don't even see it posted on their website yet."
The FDA now officially considers cannabis highly dangerous, with no medical use.
“This has big implications,” said U.S. Rep. John Mica, R-Fla., who is leading the oversight hearing on marijuana research as part of an examination of changing societal attitudes about the drug.
The FDA has reviewed the plant's status twice since the turn of the century -- in 2001 and 2006 -- both times concluding it should remain in the Schedule 1 category, Throckmorton said.
The DEA has since been petitioned to change marijuana’s classification and “that has been sent to us and we’re in the process of conducting an eight-factor analysis,” Throckmorton told Mica.
The classification is the harshest of the five DEA drug schedules and comes with the most restrictions. Other Schedule 1 drugs include heroin, LSD and MDMA (otherwise known as "ecstasy").
Mica is chairman of the House Oversight Committee’s government operations panel. A change in schedule could help reconcile some of the differences between federal laws and looser state laws. Twenty-three states and the District of Columbia permit medical marijuana and two, Washington and Colorado, allow recreational use. (New York became the 23rd this week.)
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