UTIBRON NEOHALER
LOE ApproachingNDAINHALATIONPOWDER
Approved
Oct 2015
Lifecycle
LOE Approaching
Competitive Pressure
15/100
Data completeness
2/8 — Basic
Drug data last refreshed 3d ago · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
UTIBRON NEOHALER is a combination inhalation powder approved by FDA in October 2015 for chronic obstructive pulmonary disease (COPD) maintenance therapy. The product is a small-molecule dual bronchodilator delivered via dry powder inhaler, designed to improve airflow and reduce exacerbations in COPD patients. Specific mechanism of action details are not available in current data.
LOE Approaching2.5 years to LOE
Product faces LOE in late 2028 with moderate competitive pressure (15 competitors), signaling downsizing of brand team and shift toward generic transition planning.
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.
Why This Matters for Your Career
LOE in ~3 years — strategic planning for patent cliff underway
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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.