Product image of Modiodal (Modafinil) supplied by GNH India

Modiodal

Active Ingredient:
Modafinil
Origin:
EU

Modiodal (Modafinil)

Modafinil, the active ingredient in Modiodal, is a eugeroic (wakefulness‑promoting agent) presented as an oral dosage form for oral administration. It is used to improve daytime alertness in patients with narcolepsy, obstructive sleep apnea‑related excessive daytime sleepiness, and shift work sleep disorder, and is indicated for adult patients requiring sustained wakefulness.

GNH India supplies Modiodal as a licensed, GDP‑compliant international pharmaceutical product to hospitals, pharmacies and clinics worldwide, adhering to stringent quality standards and providing reliable supply chain support for global healthcare providers.

Manufacturer / TM Owner

Neuraxpharm Pharmaceuticals S.L.

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Indications & Clinical Uses

  • Modiodal (modafinil) is prescribed for several sleep‑wake disorders where excessive daytime sleepiness is a primary symptom.
  • Narcolepsy: reduces the frequency of daytime sleep attacks, improves overall alertness, and supports better daily functioning in affected individuals.
  • Obstructive sleep apnea‑related excessive daytime sleepiness: enhances wakefulness and reduces sleepiness when used as an adjunct to standard continuous positive airway pressure (CPAP) therapy.
  • Shift work sleep disorder: helps maintain alertness and cognitive performance during scheduled work hours that conflict with the normal circadian rhythm, facilitating safer and more productive night‑time work.

How It Works

  • Modafinil promotes wakefulness primarily by inhibiting the reuptake of dopamine, thereby increasing extracellular dopamine concentrations in brain regions that regulate arousal. It also modulates additional neurotransmitter systems, including orexin, histamine, norepinephrine and serotonin pathways, which together enhance cortical activation and reduce sleep propensity. The drug’s effect on these systems is thought to increase glutamatergic transmission while decreasing GABAergic inhibition, contributing to a net excitatory state that supports sustained alertness without directly stimulating adrenergic receptors.

Side Effects

Modiodal may be associated with a range of adverse reactions, which are generally categorized by frequency and severity.

Common Side Effects

  • Headache
  • Nausea
  • Insomnia
  • Dry mouth

Serious or Rare Side Effects

  • Rash or Stevens‑Johnson syndrome
  • Psychiatric symptoms such as mania or hallucinations
  • Cardiac arrhythmia

Precautions & Warnings

  • Before initiating therapy, clinicians should consider several safety measures.
  • Cardiovascular assessment: evaluate blood pressure and heart rhythm in patients with known cardiac disease.
  • Psychiatric history review: avoid use in individuals with uncontrolled psychosis or severe anxiety.
  • Concomitant medication review: assess for drugs that affect CYP3A4 metabolism.
  • Liver function monitoring: periodic testing is advised for patients with hepatic impairment.
  • Avoid use in known hypersensitivity: discontinue if allergic reaction occurs.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Modiodal can interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, erythromycin) – may increase plasma concentrations.
  • Hormonal contraceptives – may reduce contraceptive efficacy.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, carbamazepine) – may lower drug exposure.
  • Antihypertensives – may enhance blood‑pressure‑lowering effect.
  • Alcohol – can increase central nervous system side effects.
  • Caffeine – may exacerbate insomnia or nervousness.

Frequently Asked Questions

Modiodal contains modafinil and is indicated for the treatment of excessive daytime sleepiness associated with narcolepsy, obstructive sleep apnea‑related sleepiness, and shift work sleep disorder. In each case the medication aims to improve wakefulness and functional alertness during the day.

Modafinil primarily blocks the reuptake of dopamine, raising its extracellular levels in brain areas that regulate arousal. It also influences orexin, histamine, norepinephrine and serotonin pathways, and enhances glutamatergic activity while reducing GABA‑mediated inhibition, producing a net excitatory effect that supports sustained alertness.

The prescribed dose of Modiodal is determined by the treating physician based on the individual’s clinical condition, age, and response to therapy. Patients should follow the prescriber’s instructions exactly and should not adjust the dose without medical guidance.

Safety data for modafinil in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To place an order, submit an enquiry on the Modiodal product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Modiodal (modafinil) and its R‑enantiomer armodafinil belong to the same drug class and share a similar efficacy profile. Compared with older stimulants such as methylphenidate, modafinil generally has a lower risk of cardiovascular stimulation and fewer reports of abuse, although individual response can vary.

Modiodal should be stored at ambient temperature, preferably below 25 °C. Keep the tablets in the original blister pack, protect them from moisture and direct sunlight, and ensure the container is tightly closed to maintain product stability.

Modiodal is taken orally, usually with a glass of water. The tablet should be swallowed whole and not chewed or crushed. It can be taken with or without food, but patients should follow the specific timing instructions provided by their prescriber.

Serious adverse events, although rare, include severe skin reactions such as Stevens‑Johnson syndrome, psychiatric disturbances like mania or hallucinations, and cardiac arrhythmias. Patients should seek immediate medical attention if they notice rash, mood changes, or irregular heartbeats.

Modiodal should not be used by individuals with known hypersensitivity to modafinil or any of its excipients, by patients with uncontrolled hypertension, severe cardiac disease, or active psychiatric disorders, and it is contraindicated in those taking certain CYP3A4‑inhibiting medications without medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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