Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 204153

LUZU (LULICONAZOLE)
1% Marketing Status: Prescription

Active Ingredient: LULICONAZOLE
Proprietary Name: LUZU
Dosage Form; Route of Administration: CREAM; TOPICAL
Strength: 1%
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N204153
Product Number: 001
Approval Date: Nov 14, 2013
Applicant Holder Full Name: MEDICIS PHARMACEUTICAL CORP
Marketing Status:  Prescription
Patent and Exclusivity Information

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