Product image of Memantine Biogaran (Memantine Hydrochloride) supplied by GNH India

Memantine Biogaran

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantine Biogaran (Memantine Hydrochloride)

Memantine Hydrochloride, the active ingredient in Memantine Biogaran, is an NMDA receptor antagonist presented as an oral dosage form for oral use. It is indicated for the symptomatic treatment of moderate to severe Alzheimer’s disease in adult patients.

GNH India supplies Memantine Biogaran as a licensed, GDP‑compliant international pharmaceutical product sourced from the European Union, serving hospitals, pharmacies and clinics worldwide with consistent quality and regulatory compliance. Our supply chain adheres to stringent temperature‑controlled logistics and documentation practices to ensure product integrity from manufacture to end‑user.

Manufacturer / TM Owner

Biogaran

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Indications & Clinical Uses

Memantine Biogaran is used within the Alzheimer’s disease therapeutic pathway to address cognitive decline in patients with moderate to severe disease.

  • Alzheimer’s disease (moderate to severe): helps improve cognition, daily functioning, and overall clinical status in affected adults.

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, it reduces excessive calcium influx caused by glutamate over‑activation, thereby limiting excitotoxic neuronal injury that contributes to cognitive decline in Alzheimer’s disease.

Side Effects

Memantine Biogaran may be associated with a range of adverse reactions.

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Headache: mild to moderate intensity.
  • Constipation: reduced bowel movements.
  • Confusion: temporary disorientation.
  • Hypertension: elevated blood pressure readings.

Serious or Rare Side Effects

  • Seizures: convulsive episodes requiring immediate medical attention.
  • Cardiac arrhythmia: irregular heart rhythm.
  • Severe rash or skin reactions: including Stevens‑Johnson syndrome.
  • Hepatic dysfunction: signs of liver injury.
  • Suicidal ideation: thoughts of self‑harm.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety factors.

  • Renal impairment: adjust dose or monitor renal function.
  • Hepatic impairment: use with caution in patients with liver disease.
  • Concomitant NMDA antagonists: avoid combined use to prevent additive neuro‑toxicity.
  • History of seizures: assess risk and monitor closely.
  • Cardiovascular disease: monitor blood pressure and heart rate.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Memantine may interact with other medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Amantadine: combined NMDA antagonism may increase neuro‑toxicity.
  • CNS depressants (e.g., benzodiazepines): may enhance sedation.
  • High‑dose antihypertensives: risk of excessive blood pressure reduction.

Moderate Interactions (Monitor Closely)

  • Acetylcholinesterase inhibitors (e.g., donepezil): may affect overall cognitive response.
  • Diuretics: monitor electrolyte balance.
  • Drugs cleared renally (e.g., metformin): adjust dosing if renal function declines.

Frequently Asked Questions

Memantine Biogaran contains memantine hydrochloride and is prescribed for the symptomatic treatment of moderate to severe Alzheimer’s disease, helping to improve cognition and daily functioning in adult patients.

Memantine acts as a non‑competitive antagonist at NMDA receptors, reducing excessive calcium influx caused by glutamate over‑activation. This limits excitotoxic neuronal damage that contributes to cognitive decline in Alzheimer’s disease.

The appropriate dose of Memantine Biogaran is determined by the prescribing clinician based on the patient’s condition, renal function, and response to therapy. Patients should follow the prescriber’s instructions exactly.

Safety data for memantine during pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies any potential risk to the fetus or infant, and decisions should be made in consultation with a healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com with 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 necessary import documentation.

Memantine belongs to the NMDA receptor antagonist class, whereas other approved agents such as donepezil are acetylcholinesterase inhibitors. Memantine targets glutamatergic excitotoxicity, offering a complementary mechanism that may be used alone or in combination with cholinergic agents.

Memantine Biogaran should be stored at room temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight, and extreme temperatures to maintain its stability.

Memantine Biogaran is taken orally, usually as a tablet, with or without food as directed by the prescriber. Swallow the tablet whole with water and do not crush or chew unless specifically instructed.

Serious risks include seizures, cardiac arrhythmias, severe skin reactions such as Stevens‑Johnson syndrome, hepatic dysfunction, and emergence of suicidal thoughts. Patients should be monitored closely for these events and seek immediate medical attention if they occur.

Memantine Biogaran is contraindicated in patients with known hypersensitivity to memantine or any excipients, and should be used with caution in individuals with severe renal or hepatic impairment, uncontrolled hypertension, or a history of seizures.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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