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FDA Approves Mayne’s Halobetasol Foam For Adolescents

Australian Company Strengthens Its Dermatology Portfolio With US Lexette Nod

 
• By Akriti Seth

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. 

Dermatology
Mayne Pharma markets more than twenty dermatology products in the US • Source: Alamy

Australia-based Mayne Pharma USA has received US Food and Drug Administration approval for its Lexette (halobetasol propionate) 0.05% foam, “a super potent topical corticosteroid” for the treatment of plaque psoriasis for use in adolescents.

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