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US FDA Rides Different Monograph System In Second Roundup Of Oral Phenylephrine Efficacy

 
• By Malcolm Spicer

“One of the things that we're particularly excited about under monograph reform is it does give us the opportunity to move things along a little bit more quickly,” says FDA Office of Nonprescription Drugs director Theresa Michele during NDAC meeting.

• Source: Shutterstock

The US Food and Drug Administration’s second meeting to ask an advisory committee about oral phenylephrine’s efficacy as a nasal decongestant won’t end with the ingredient’s critics and supporters agreeing.

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More from Policy & Regulation

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