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FDA Drug Approval, N019079, FLAREX
FDA Drug Approval, N019079, FLAREX
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NDA: 019079
Company: HARROW EYE
Drug Name: FLAREX
Active Ingredients: FLUOROMETHOLONE ACETATE
Strength: 0.1%
Dosage Form/Route: SUSPENSION/DROPS;OPHTHALMIC
Action Date: 02/11/1986
Marketing Status: Prescription
Submission Classification: Type 2 - New Active Ingredient
Company: HARROW EYE
Drug Name: FLAREX
Active Ingredients: FLUOROMETHOLONE ACETATE
Strength: 0.1%
Dosage Form/Route: SUSPENSION/DROPS;OPHTHALMIC
Action Date: 02/11/1986
Marketing Status: Prescription
Submission Classification: Type 2 - New Active Ingredient
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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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