FDA Panel Shoots Down Intellipharma Opioid

Independent advisers said there wasn't enough evidence to approve Intellipharma's opioid painkiller as there wasn't adequate data on the abuse potential of the drug.
July 26, 2017

A U.S. FDA panel of independent advisers said there was not enough evidence to support the approval of Toronto-based Intellipharmaceutics International's long-acting opioid painkiller, according to a Reuters article.

The painkiller was developed as an abuse-deterrent version of Purdue Pharma's OxyContin, which already has tamper-resistant properties. The drug has a blue dye that is emitted if the tablet is manipulated, which could help identify abusers, and a nasal irritant to discourage misuse, the story said.

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