Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 210566

LEXETTE (HALOBETASOL PROPIONATE)
0.05%
Marketing Status: Prescription
Active Ingredient: HALOBETASOL PROPIONATE
Proprietary Name: LEXETTE
Dosage Form; Route of Administration: AEROSOL, FOAM; TOPICAL
Strength: 0.05%
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N210566
Product Number: 001
Approval Date: May 24, 2018
Applicant Holder Full Name: MAYNE PHARMA LLC
Marketing Status:  Prescription
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