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FDA Drug Approval, N020273, DOVONEX
FDA Drug Approval, N020273, DOVONEX
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NDA: 020273
Company: LEO PHARMA AS
Drug Name: DOVONEX
Active Ingredients: CALCIPOTRIENE
Strength: 0.005%
Dosage Form/Route: OINTMENT;TOPICAL
Action Date: 12/29/1993
Marketing Status: Prescription
Submission Classification: Type 1 - New Molecular Entity
Company: LEO PHARMA AS
Drug Name: DOVONEX
Active Ingredients: CALCIPOTRIENE
Strength: 0.005%
Dosage Form/Route: OINTMENT;TOPICAL
Action Date: 12/29/1993
Marketing Status: Prescription
Submission Classification: Type 1 - New Molecular Entity
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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