tiotropium 2.5 MCG / olodaterol 2.5 MCG per ACTUAT Metered Dose Inhalation Spray, 10 ACTUAT

RxCUI: 2166927
RxNorm name: tiotropium 2.5 MCG / olodaterol 2.5 MCG per ACTUAT Metered Dose Inhalation Spray, 10 ACTUAT
Display name: tiotropium 2.5 MCG / olodaterol 2.5 MCG per ACTUAT Metered Dose Inhalation Spray, 10 ACTUAT
Full name: tiotropium 2.5 MCG / olodaterol 2.5 MCG per ACTUAT Metered Dose Inhalation Spray, 10 ACTUAT
Term type: PSN
Status: DailyMed mapping
Updated: 2026-06-04 23:38:45

RxNav Current And Historical NDCs#

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UNII Substances#

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openFDA label cross-check#

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

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Stiolto Respimat	TIOTROPIUM BROMIDE AND OLODATEROL	Boehringer Ingelheim Pharmaceuticals, Inc.	01e15aee-40e0-23f3-537f-c96dd63e2cb1	2025-06-30	Warnings, Adverse reactions	Exact identifier rxcui: 2166927

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 · 1 matching rows.

Set ID, RxNorm mappings, Terms table
Set ID	RxNorm mappings	Terms	SPL version	Label	Effective
01e15aee-40e0-23f3-537f-c96dd63e2cb1	tiotropium 2.5 MCG / olodaterol 2.5 MCG per ACTUAT Metered Dose Inhalation Spray, 10 ACTUAT [PSN] · 10 ACTUAT olodaterol 0.0025 MG/ACTUAT / tiotropium 0.0025 MG/ACTUAT Inhalation Spray [SCD] · olodaterol 2.5 MCG (as olodaterol HCl 2.736 MCG) / tiotropium 2.5 MCG (as tiotropium bromide 3.124 MCG) per ACTUAT Metered Dose Inhalation Spray, 10 ACTUAT [SY] · olodaterol 2.5 MCG / tiotropium 2.5 MCG per ACTUAT Metered Dose Inhalation Spray, 10 ACTUAT [SY]	4	16	These highlights do not include all the information needed to use STIOLTO RESPIMAT safely and effectively. See full prescribing information for STIOLTO RESPIMAT. STIOLTO ® RESPIMAT ® (tiotropium bromide and olodaterol inhalation spray), for oral inhalation use Initial U.S. Approval: 2015	20250630