NDAORALTABLET, EXTENDED RELEASE
Approved
Oct 2013
Lifecycle
Peak
Competitive Pressure
30/100
Clinical Trials
20
Data completeness
3/8 — Basic
DESVENLAFAXINE (desvenlafaxine fumarate) by Teva is unknown, but is thought to be related to the potentiation of serotonin and norepinephrine in the central nervous system, through inhibition of their reuptake. First approved in 2013.
Drug data last refreshed 18h ago · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
Desvenlafaxine fumarate is an oral extended-release SNRI antidepressant that potentiates serotonin and norepinephrine in the central nervous system through reuptake inhibition. It is indicated for major depressive disorder and related mood disorders. The drug demonstrates linear, dose-proportional pharmacokinetics with steady-state achievement in 4-5 days and ~80% oral bioavailability.
Peak
Product is at peak lifecycle with moderate competitive pressure (30%), indicating stable commercial operations but limited growth opportunities.
Mechanism of Action
unknown, but is thought to be related to the potentiation of serotonin and norepinephrine in the central nervous system, through inhibition of their reuptake. Non-clinical studies have shown that desvenlafaxine is a potent and selective serotonin and norepinephrine reuptake inhibitor (SNRI). 12.2…
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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.