Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 022013

OLUX E (CLOBETASOL PROPIONATE)
0.05% Marketing Status: Prescription

Active Ingredient: CLOBETASOL PROPIONATE
Proprietary Name: OLUX E
Dosage Form; Route of Administration: AEROSOL, FOAM; TOPICAL
Strength: 0.05%
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB2
Application Number: N022013
Product Number: 001
Approval Date: Jan 12, 2007
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:  Prescription
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