Vernalis' collaboration with Tris

Latest status of the programmes for the US prescription market.

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Tuzistra® XR, the first cough cold product resulting from a development and licensing deal with Tris Pharma Inc., was approved by the FDA in April 2015. Vernalis has 4 additional products in development in its cough cold pipeline.

 

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In October 2015, Vernalis also acquired the US rights to Moxatag®, a once-a-day amoxicillin for strep throat in adult and pediatric patients 12 years of age or older and re-launched the product in Q4 2016.

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Latest News

FDA Issues a Complete Response Letter on CCP-08 NDA

Vernalis plc announced today that the US Food and Drug Administration (FDA) has issued a Complete Response Letter (CRL) regarding the New Drug Application (NDA) for CCP-08. 

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At a glance

More information on Vernalis and its pipeline ...

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To report SUSPECTED ADVERSE REACTIONS, contact Vernalis Therapeutics, Inc. at 1-855-705-9546 and drugsafety@propharmagroup.com or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch