NDAORALCAPSULE, EXTENDED RELEASE
Approved
Jul 2013
Lifecycle
Peak
Competitive Pressure
0/100
Data completeness
6/8 — Strong
FETZIMA (levomilnacipran hydrochloride) by AbbVie is unknown, but is thought to be related to the potentiation of serotonin and norepinephrine in the central nervous system, through inhibition of reuptake at serotonin and norepinephrine transporters. Approved for major depressive disorder (mdd) in adults (). First approved in 2013.
Drug data last refreshed 10h ago · AI intelligence enriched 3w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
FETZIMA (levomilnacipran hydrochloride) is an oral extended-release SNRI approved for Major Depressive Disorder in adults. It works by potentiating serotonin and norepinephrine in the central nervous system through selective reuptake inhibition at both transporters. The mechanism is thought to restore neurotransmitter balance in depression.
$0.029BPart D
PeakStable
5.8 years to LOEStable mature product with modest Medicare claims (~43k annually) indicating a niche position in the crowded depression market; likely supporting a lean commercial team.
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 reuptake at serotonin and norepinephrine transporters. Non-clinical studies have shown that levomilnacipran is a potent and selective serotonin and…
Indications (1)
Career Relevance
FETZIMA represents a stable, mature product with minimal career growth trajectory; roles are primarily in defensive commercial management and lifecycle extension strategy. This is a consolidation play rather than a growth opportunity, best suited for professionals seeking stability in a niche psychiatric segment.
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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.