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SPIRIVA HANDIHALER

LAMA DPI

Tiotropium bromide · Boehringer Ingelheim

Clinical Reference · Data reviewed June 2026

Active Medication & Mechanism

  • Tiotropium bromide monohydrate LAMA
    18 mcg per capsule (delivers a mean of 10.4 mcg from the mouthpiece in vitro at 39 L/min)

    Long-acting muscarinic antagonist (anticholinergic). Binds to M1–M3 muscarinic receptors, with slow dissociation from M3 receptors on airway smooth muscle, providing 24-hour bronchodilation.

FDA-Approved Dosing — Strength × Indication

18 mcg 2 inhalations of 1 capsule once daily (entire capsule content) → 18 mcg
COPD FDA Approved
Long-term, once-daily maintenance treatment of bronchospasm associated with COPD, including chronic bronchitis and emphysema. Also reduces COPD exacerbations.
Asthma Not Approved
Spiriva HandiHaler is not FDA-approved for asthma; Spiriva Respimat carries the asthma indication (different product and dose).

All regimens shown apply to adults (≥18 years) unless otherwise noted · verify against current labelling

Not a rescue inhaler. Not for acute bronchospasm. Per labeling, a SABA is used.

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For educational reference by healthcare professionals. Not medical advice and not for use in clinical decision-making. This workspace is not a substitute for clinical judgement, prescribing information, or product monographs — always verify doses and indications against the most current labelling. If you are a patient, do not use this site to make medication decisions — speak with your clinician.

Device images are original illustrations for identification aid only — actual devices and packaging may differ. This site is not affiliated with or endorsed by any pharmaceutical manufacturer. Clinical data last reviewed: June 2026.

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