Mazindol is a tricyclic anorexigenic agent approved for short-term obesity treatment and off-label narcolepsy management. Unlike amphetamines, it produces primarily dysphoric rather than euphoric effects, reducing abuse potential. Its dual mechanism targeting both monoamine reuptake and orexin-2 receptors makes it unique among stimulants. Common side effects include insomnia, dry mouth, anxiety, increased heart rate, and restlessness. Use with extreme caution in individuals with cardiovascular disease, hypertension, hyperthyroidism, or glaucoma.
Mazindol molecular structure diagram from the DrugsPRO substance library.
Also known as: Sanorex, Mazanor, Teronac, Terenac, Dimagrir, AN-448, 42-548
Classification
Psychoactive: Stimulant
Tag: Appetite-suppressant
Tag: Eugeroic
Tag: Imidazoisoindole
Tag: Pharmaceutical
Tag: Tricyclic compound
Effects
Increased Alertness
Restlessness
Insomnia
Dry Mouth
Increased Heart Rate
Loss Of Appetite
Wakefulness
Anxiety
Focus Enhancement
Dysphoria
Motivation Enhancement
Euphoria
Appetite Suppression
Light Sensitivity
Dehydration
Photophobia
Spontaneous Physical Sensations
Increased Libido
Routes of Administration
Oral
Dosage
Threshold: 0.5 mg
Light: 0.5-1 mg
Common: 1-2 mg
Strong: 2-3 mg
Heavy: 3+ mg
Duration
Onset: 0.5-1 h
Comeup: 0.5-1.5 h
Peak: 2-4 h
Offset: 4-8 h
After Effects: 24 h
Harm Reduction
Check interactions before mixing substances, pay attention to dose spacing and hydration, and treat all dosage guidance as approximate rather than guaranteed safe.
Sources
Substance data is aggregated from the following public harm-reduction and reference sources.
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Mazindol - DrugsPRO stoffveiledning
Mazindol: Mazindol is a tricyclic anorexigenic agent approved for short-term obesity treatment and off-label narcolepsy management. Unlike amphetamines, it produces primarily dysphoric rather than euphoric effects, reducing abuse potential. Its dual mechanism targeting both monoamine reuptake and or