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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 009112

EURAX (CROTAMITON)
10%
Marketing Status: Prescription
Active Ingredient: CROTAMITON
Proprietary Name: EURAX
Dosage Form; Route of Administration: LOTION; TOPICAL
Strength: 10%
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AT
Application Number: N009112
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: JOURNEY MEDICAL CORP
Marketing Status:  Prescription
Patent and Exclusivity Information
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