NDAINHALATIONSPRAY, METERED
Approved
Oct 2011
Lifecycle
Peak
Competitive Pressure
8/100
Clinical Trials
3
Data completeness
5/8 — Partial
Drug data last refreshed 10h ago · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
COMBIVENT RESPIMAT is a fixed-dose combination of ipratropium bromide (anticholinergic) and albuterol (beta-2 agonist) delivered via metered-spray inhalation. It is indicated for maintenance treatment of airflow obstruction in patients with chronic obstructive pulmonary disease (COPD). The dual mechanism provides bronchodilation through complementary pathways—ipratropium blocks acetylcholine receptors while albuterol stimulates beta-2 receptors.
$0.456BPart D
PeakStable
4.2 years to LOEProduct is at peak commercial performance with $456M in Part D spending and 683,764 annual claims, indicating a mature franchise with stable team requirements.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (3)
Ventilator Adapters for Combivent Respimat
Started Oct 2013
11 enrolled
Pulmonary Disease, Chronic Obstructive
Combivent Respimat 1-year Safety Study in Patients With Chronic Obstructive Pulmonary Disease
Started Nov 2009
470 enrolled
Pulmonary Disease, Chronic Obstructive
4 Week 2 Way Crossover Double Blind Treatment Phase With Combivent CFC Versus Albuterol Followed by a 4 Week Open Label Combivent Respimat When All Drugs Are Used for Symptom Relief as Needed in Pts With Moderate to Severe Asthma
Started Dec 2008
226 enrolled
Asthma
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.