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FDA Drug Approval, N018748, LOPROX
FDA Drug Approval, N018748, LOPROX
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NDA: 018748
Company: MEDIMETRIKS PHARMS
Drug Name: LOPROX
Active Ingredients: CICLOPIROX
Strength: 0.77%
Dosage Form/Route: CREAM;TOPICAL
Action Date: 12/30/1982
Marketing Status: Prescription
Submission Classification: Type 1 - New Molecular Entity
Company: MEDIMETRIKS PHARMS
Drug Name: LOPROX
Active Ingredients: CICLOPIROX
Strength: 0.77%
Dosage Form/Route: CREAM;TOPICAL
Action Date: 12/30/1982
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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