FDA.reportPublic FDA data

cyclosporine 0.5 MG/ML Ophthalmic Suspension [Restasis]

RxCUI
402092
RxNorm name
cyclosporine 0.5 MG/ML Ophthalmic Suspension [Restasis]
Display name
cyclosporine 0.5 MG/ML Ophthalmic Suspension [Restasis]
Full name
cyclosporine 0.5 MG/ML Ophthalmic Suspension [Restasis]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:39:03

RxNav Current And Historical NDCs#

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No records found.

UNII Substances#

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No records found.

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Restasis MultiDoseCYCLOSPORINEAllergan, Inc.7224d810-bb96-4682-a942-3355e6e8061a2025-08-21Warnings, Adverse reactionsExact identifier
rxcui: 402092

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 1 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
7224d810-bb96-4682-a942-3355e6e8061aRestasis 0.05 % Ophthalmic Emulsion [PSN] · cyclosporine 0.5 MG/ML Ophthalmic Suspension [Restasis] [SBD] · Restasis 0.05 % Ophthalmic Emulsion [SY] · Restasis 0.05 % Ophthalmic Suspension [SY] · Restasis 0.5 MG/ML Ophthalmic Suspension [SY]515These highlights do not include all the information needed to use RESTASIS MULTIDOSE safely and effectively. See full prescribing information for RESTASIS MULTIDOSE . RESTASIS MULTIDOSE ® ( cyclosporine ophthalmic emulsion ) 0.05% , f or topical ophthalmic use Initial U.S. Approval: 198320250821