FDA.reportPublic FDA data

Combigan 0.2 % / 0.5 % Ophthalmic Solution

RxCUI
861637
RxNorm name
Combigan 0.2 % / 0.5 % Ophthalmic Solution
Display name
Combigan 0.2 % / 0.5 % Ophthalmic Solution
Full name
Combigan 0.2 % / 0.5 % Ophthalmic Solution
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:39:29

RxNav Current And Historical NDCs#

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UNII Substances#

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openFDA label cross-check#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
COMBIGANBRIMONIDINE TARTRATE, TIMOLOL MALEATEAllergan, Inc.feaf1480-a4b8-4486-992a-96be3a5962432026-03-17Warnings, Adverse reactionsExact identifier
rxcui: 861637

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 2 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
feaf1480-a4b8-4486-992a-96be3a596243Combigan 0.2 % / 0.5 % Ophthalmic Solution [PSN] · brimonidine tartrate 2 MG/ML / timolol 5 MG/ML Ophthalmic Solution [Combigan] [SBD] · Combigan (brimonidine tartrate 0.2 % / timolol 0.5 % ) Ophthalmic Solution [SY]322These highlights do not include all the information needed to use COMBIGAN safely and effectively. See full prescribing information for COMBIGAN. COMBIGAN ® (brimonidine tartrate and timolol maleate ophthalmic solution) 0.2%/0.5% , f or topical ophthalmic use Initial U.S. Approval: 200720260317
8c641b6c-3335-4ec3-89b9-2d97a8901062Combigan 0.2 % / 0.5 % Ophthalmic Solution [PSN] · brimonidine tartrate 2 MG/ML / timolol 5 MG/ML Ophthalmic Solution [Combigan] [SBD] · Combigan (brimonidine tartrate 0.2 % / timolol 0.5 % ) Ophthalmic Solution [SY]31These highlights do not include all the information needed to use COMBIGAN ® safely and effectively. See full prescribing information for COMBIGAN ® . COMBIGAN ® (brimonidine tartrate/timolol maleate ophthalmic solution) 0.2%/0.5% Initial U.S. Approval: 200720110415