FDA on hydrocodone

October 8, 2014

THE US Food and Drug Administration (FDA) has said new prescribing requirements for hydrocodone combination products came into effect this week, which saw the products re-scheduled from Schedule 3 to Schedule 2. A prescriber had to issue a new prescription if the patient needed more medication, with phone in refills no longer allowed, regulatory programs deputy centre director Douglas Throckmorton said. This would help limit the risks of these products, and strove to achieve balance between risk of abuse and the need for access to important medications, he said.

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Pharmacy Daily | FDA on hydrocodone

FDA on hydrocodone

Other recent headlines

WA group stocks vapes

Fujitsu to protect against cyber threats

PD breaking news – Queensland pharmacies scope of practice pilot expanded

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES