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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 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
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.

Links

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Mazindol - Guía de sustancias de DrugsPRO

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

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