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The FDA's request for reclassification must be approved by administration officials in the Department of Health and Human Services. News of the FDA decision was applauded by lawmakers from states that have been plagued by prescription drug abuse, many who have been prodding the agency to take action for months. "Today was a tremendous step forward in fighting the prescription drug abuse epidemic that has ravaged West Virginia and our country," said Democratic Sen. Joe Senator Manchin, in a statement. "Rescheduling hydrocodone from a Schedule III to a Schedule II drug will help prevent these highly addictive drugs from getting into the wrong hands and devastating families and communities Sen. Charles Schumer of New York noted that the FDA's own expert panel recommended the reclassification more than nine months ago. "Each day that passes means rising abuse, and even death, at the hands of hydrocodone-based drugs," Schumer said in a statement. Still, Thursday's action is likely to face opposition from many physicians and pharmacists. Some professional groups argue that the tighter restrictions could have unintended consequences, burdening doctors with extra work and driving addicted patients to obtain the drugs illegally.
[Associated
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