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Sanofi’s Nasacort AQ Rx-To-OTC Switch Under FDA Review

This article was originally published in The Tan Sheet

Executive Summary

FDA’s Nonprescription Drugs Advisory Committee will meet July 31 to discuss Sanofi’s application to switch the intranasal corticosteroid Nasacort AQ to OTC sale, to be indicated for relief of hay fever symptoms in adults and children.

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Nasacort AQ Switch Rides On “Evolution Of Data” – Sanofi CMO

Charles Hugh-Jones, Sanofi’s chief medical officer for North America, says the firm will present clinical and consumer use data to allay concerns about the safety of intranasal corticosteroids, at the upcoming FDA advisory committee meeting to discuss the Rx-to-OTC switch of Nasacort AQ.

Nasacort AQ Switch Rides On “Evolution Of Data” – Sanofi CMO

Charles Hugh-Jones, Sanofi’s chief medical officer for North America, says the firm will present clinical and consumer use data to allay concerns about the safety of intranasal corticosteroids, at the upcoming FDA advisory committee meeting to discuss the Rx-to-OTC switch of Nasacort AQ.

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