FDA.reportPublic FDA data

omidenepag isopropyl 0.02 MG/ML Ophthalmic Solution [Omlonti]

RxCUI
2612704
RxNorm name
omidenepag isopropyl 0.02 MG/ML Ophthalmic Solution [Omlonti]
Display name
omidenepag isopropyl 0.02 MG/ML Ophthalmic Solution [Omlonti]
Full name
omidenepag isopropyl 0.02 MG/ML Ophthalmic Solution [Omlonti]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:38:55

RxNav Current And Historical NDCs#

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No records found.

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.

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

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
OmlontiOMIDENEPAG ISOPROPYLOcuvex Therapeutics, Inc.4258e437-7e92-4b09-baf1-01cb158cfc052025-04-21Warnings, Adverse reactionsExact identifier
rxcui: 2612704

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
4258e437-7e92-4b09-baf1-01cb158cfc05OMLONTI 0.002 % Ophthalmic Solution [PSN] · omidenepag isopropyl 0.02 MG/ML Ophthalmic Solution [Omlonti] [SBD] · OMLONTI 0.002 % Ophthalmic Solution [SY] · Omlonti 0.02 MG/ML Ophthalmic Solution [SY]43These highlights do not include all the information needed to use OMLONTI ® safely and effectively. See full prescribing information for OMLONTI ® . OMLONTI ® (omidenepag isopropyl ophthalmic solution) 0.002%, for topical ophthalmic use Initial U.S. Approval: 202220250421