Product image of Memantina Gp (Memantine Hydrochloride) supplied by GNH India

Memantina Gp

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantina Gp (Memantine Hydrochloride)

Memantine Hydrochloride, the active ingredient in Memantina Gp, is a NMDA receptor antagonist presented as an oral tablet for oral use. It is used to treat Alzheimer’s disease in adult patients.
GNH India supplies Memantina Gp as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Gp – Genéricos Portugueses, Lda.

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Indications & Clinical Uses

Memantine Hydrochloride is indicated for disorders of the central nervous system that involve glutamatergic excitotoxicity, primarily Alzheimer’s disease.

  • Alzheimer’s disease (mild to moderate): helps maintain cognitive function and daily living activities.
  • Alzheimer’s disease (moderate to severe): may slow functional decline and improve global clinical status.
  • Alzheimer’s disease with behavioral disturbances: can reduce agitation and improve overall patient behavior.

How It Works

  • Memantine Hydrochloride acts as a non‑competitive antagonist at the N‑methyl‑D‑aspartate (NMDA) receptor. By binding to the receptor-associated ion channel at a site distinct from the glutamate binding site, it reduces excessive calcium influx caused by prolonged glutamate activation, thereby limiting excitotoxic neuronal injury that contributes to cognitive decline in Alzheimer’s disease.

Side Effects

Common Side Effects

  • Dizziness: mild to moderate sensation of light‑headedness.
  • Headache: transient cranial pain.
  • Constipation: reduced bowel motility.
  • Confusion: occasional disorientation.
  • Fatigue: general tiredness.
  • Hypertension: elevated blood pressure readings.

Serious or Rare Side Effects

  • Seizures: convulsive episodes requiring medical attention.
  • Cardiac arrhythmia: irregular heart rhythm.
  • Severe hepatic injury: signs of liver dysfunction.
  • Stevens‑Johnson syndrome: serious skin reaction.
  • Suicidal ideation: thoughts of self‑harm.
  • Severe rash or hypersensitivity: extensive skin eruption.

Precautions & Warnings

Memantine Hydrochloride should be used with caution in specific clinical situations.

  • Renal impairment: adjust dose or monitor renal function.
  • Hepatic impairment: consider dose reduction.
  • History of seizures: monitor for increased seizure activity.
  • Cardiovascular disease: observe blood pressure and heart rhythm.
  • Concomitant NMDA agonists: avoid combined use due to antagonistic effects.
  • Store below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Memantine Hydrochloride can interact with several medication classes.

Major Interactions (Avoid)

  • Amantadine: combined NMDA antagonism may increase neuropsychiatric effects.
  • Other NMDA antagonists (e.g., ketamine): additive central nervous system depression.

Moderate Interactions (Monitor Closely)

  • Anticholinesterase inhibitors (e.g., donepezil): may alter efficacy of each agent.
  • Antihypertensive drugs: potential additive blood pressure lowering.
  • Diuretics: monitor electrolyte balance.
  • SSRIs or SNRIs: watch for increased risk of confusion or dizziness.

Frequently Asked Questions

Memantina Gp contains memantine hydrochloride, which is prescribed to treat Alzheimer’s disease. It helps preserve cognitive function and daily living abilities in patients with mild to severe disease by reducing neuronal excitotoxic damage.

Memantine hydrochloride works as a non‑competitive antagonist of the NMDA receptor. By blocking the receptor’s ion channel, it limits excessive calcium entry caused by overstimulation with glutamate, thereby protecting neurons from excitotoxic injury that contributes to dementia progression.

The dosage of Memantina Gp is determined by the prescribing clinician based on the patient’s clinical condition, renal function, and treatment response. The prescriber will set the appropriate strength and titration schedule.

Safety data for memantine hydrochloride in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made by a qualified healthcare professional.

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

Memantina Gp (memantine) belongs to the NMDA‑receptor antagonist class, whereas drugs such as donepezil or rivastigmine are acetylcholinesterase inhibitors. Memantine targets glutamate‑mediated excitotoxicity, offering a complementary mechanism that may be used alone or together with cholinesterase inhibitors for broader symptom control.

Memantina Gp should be stored below 25 °C in its original packaging, protected from moisture and direct sunlight. Keep the product out of reach of children and avoid exposing it to extreme temperatures.

Memantina Gp is taken orally, usually with or without food, as directed by the prescriber. The tablet should be swallowed whole with water and not crushed or chewed unless specifically instructed.

Serious risks include seizures, severe cardiac arrhythmias, hepatic injury, Stevens‑Johnson syndrome, and suicidal thoughts. Patients should be monitored for any new or worsening neurological or dermatological symptoms and seek immediate medical attention if they occur.

Memantina Gp is contraindicated in patients with known hypersensitivity to memantine hydrochloride or any of its excipients. Caution is also advised for individuals with uncontrolled severe renal or hepatic impairment, active seizures, or those taking other NMDA‑agonist agents.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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