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Helps diagnose bronchial airway hyperreactivity. Sold as Provocholine. Every FDA application for this active ingredient.
As of Nov 15, 2026, FDA lists 1 application for Methacholine Chloride (sold as Provocholine), first approved Oct 31, 1986, with 1 new use approved and 0 published complete response letters.
First approved: Oct 31, 1986
Applications: 1
New uses approved: 1
Complete response letters: 0
Medicare spending, 2025: $90K
First approved in Japan: Jan 22, 2016
Medicare Spending
CMS Part D and Part B, 2025, before manufacturer rebates; matched by generic name
Product
Part
Spending, 2025
Change
Beneficiaries
Provocholine
Part B
$90K
+18%
1,741
Approvals in Japan (PMDA)
First approved in Japan 351 months after the US. PMDA's English list since 2008, matched by ingredient; see all Japanese approvals
Provocholine, new ingredientDrugs with a new active ingredient indicated for tests in the diagnosis of bronchial airway hyperresponsiveness. · Santen Pharmaceutical Co., Ltd. · Jan 22, 2016
Clinical Trials
9 open or ongoing studies name this ingredient as an intervention, including as a comparator; newest first. See all
Applications, approvals and products come from FDA's Drugs@FDA data files, refreshed weekly, grouped by active ingredient as FDA spells it. Complete response letters are FDA's published letters. Medicare spending is CMS's Part D and Part B dashboard, matched to this ingredient by generic name; shortages are FDA's shortage list, matched by application number; clinical trials are ClinicalTrials.gov studies naming the ingredient as an intervention, refreshed daily; safety programs are FDA's REMS list, matched by application number or, for shared programs, by ingredient.Drugs@FDA