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FDA Drug Approval, N017823, HALOG
FDA Drug Approval, N017823, HALOG
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NDA: 017823
Company: SUN PHARM INDS INC
Drug Name: HALOG
Active Ingredients: HALCINONIDE
Strength: 0.1%
Dosage Form/Route: SOLUTION;TOPICAL
Action Date: 05/04/1977
Marketing Status: Discontinued
Submission Classification: Type 3 - New Dosage Form
Company: SUN PHARM INDS INC
Drug Name: HALOG
Active Ingredients: HALCINONIDE
Strength: 0.1%
Dosage Form/Route: SOLUTION;TOPICAL
Action Date: 05/04/1977
Marketing Status: Discontinued
Submission Classification: Type 3 - New Dosage Form
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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