FDA.reportPublic FDA data

latanoprost 0.005 % / netarsudil 0.02 % Ophthalmic Solution

RxCUI
2119701
RxNorm name
latanoprost 0.005 % / netarsudil 0.02 % Ophthalmic Solution
Display name
latanoprost 0.005 % / netarsudil 0.02 % Ophthalmic Solution
Full name
latanoprost 0.005 % / netarsudil 0.02 % Ophthalmic Solution
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:16

RxNav Current And Historical NDCs#

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UNII Substances#

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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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RocklatanNETARSUDIL AND LATANOPROST OPHTHALMIC SOLUTION, 0.02%/0.005%Alcon Laboratories, Inc.b1d71f41-be06-4a08-94d4-e352198f09c22026-08-27Warnings, Adverse reactionsExact identifier
rxcui: 2119701

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
b1d71f41-be06-4a08-94d4-e352198f09c2netarsudil 0.02 % / latanoprost 0.005 % Ophthalmic Solution [PSN] · latanoprost 0.05 MG/ML / netarsudil 0.2 MG/ML Ophthalmic Solution [SCD] · latanoprost 0.005 % / netarsudil 0.02 % Ophthalmic Solution [SY]314These highlights do not include all the information needed to use ROCKLATAN ® safely and effectively. See full prescribing information for ROCKLATAN ® . ROCKLATAN ® (netarsudil and latanoprost ophthalmic solution) 0.02%/0.005%, for topical ophthalmic use Initial U.S. Approval: 201920260120