EXOSURF NEONATAL
LOE ApproachingNDAINTRATRACHEALFOR SUSPENSIONPriority Review
Approved
Aug 1990
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Data completeness
1/8 — Limited
Priority Review
Drug data last refreshed 4d ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
EXOSURF NEONATAL is an intratracheal suspension approved in 1990 for neonatal respiratory distress syndrome, a critical condition in premature infants. The product is a synthetic pulmonary surfactant replacement therapy administered directly into the lungs to restore surface-active properties and improve respiratory function. It represents a foundational therapeutic approach in neonatal critical care.
LOE Approaching
Product approaching loss of exclusivity with moderate competitive pressure (30%), indicating potential team downsizing and transition to generic/maintenance phase activities.
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.
Career Relevance
Working on EXOSURF NEONATAL offers limited growth opportunities given its LOE-approaching status and zero currently linked job postings. Career progression is more likely in transition, portfolio, or legacy product management roles rather than expansion or launch activities.
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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.