IOPIDINE 1% (APRACLONIDINE HYDROCHLORIDE OPHTHALMIC SOLUTION)
Summary
FDA approved IOPIDINE 1% (APRACLONIDINE HYDROCHLORIDE OPHTHALMIC SOLUTION) by HARROW EYE. NDA (New Drug) approval (Labeling) on 2026-03-18. SOLUTION/DROPS, OPHTHALMIC.
Details
Source
Drug Approval
External ID
NDA019779-28
Action Date
2026-03-18
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
IOPIDINE 1% (generic: APRACLONIDINE HYDROCHLORIDE OPHTHALMIC SOLUTION), SOLUTION/DROPS, OPHTHALMIC. Application: NDA019779
Company
Context & Analysis
HARROW EYE has 7 FDA actions in our database.
Frequently Asked Questions
How often does HARROW EYE have FDA actions?
HARROW EYE has 7 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA019779-28" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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