FDA Drug Approval, N019779, IOPIDINE

FDA Drug Approval, N019779, IOPIDINE

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NDA: 019779
Company: HARROW EYE
Drug Name: IOPIDINE
Active Ingredients: APRACLONIDINE HYDROCHLORIDE
Strength: EQ 1% BASE
Dosage Form/Route: SOLUTION/DROPS;OPHTHALMIC
Action Date: 12/31/1987
Marketing Status: Prescription
Submission Classification: Type 1 - New Molecular Entity

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