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FDA Approves Mayne’s Halobetasol Foam For Adolescents

Australian Company Strengthens Its Dermatology Portfolio With US Lexette Nod

Executive Summary

Mayne Pharma has announced receiving US FDA approval for its Lexette (halobetasol propionate) 0.05% foam for the treatment of plaque psoriasis for use in adolescents. With Lexette, Mayne now markets more than twenty dermatology products in the US including four branded products. 

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