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

Memantine Sandoz

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantine Sandoz (Memantine Hydrochloride)

Memantine, the active ingredient in Memantine Sandoz, is a NMDA receptor antagonist presented as a tablet for oral use. It is used to treat cognitive symptoms of Alzheimer’s disease in adults.
GNH India supplies Memantine Sandoz as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Sandoz N.V.

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Indications & Clinical Uses

  • Memantine acts on the glutamatergic pathway and is indicated for the treatment of Alzheimer’s disease.
  • Alzheimer's disease: helps improve cognition and functional abilities in patients with mild to moderate disease.

How It Works

  • Memantine hydrochloride binds to the NMDA (N‑methyl‑D‑aspartate) receptor at a site distinct from the glutamate binding site, acting as a non‑competitive antagonist. By reducing excessive calcium influx, it limits excitotoxic neuronal injury and helps preserve synaptic function in the brain.

Side Effects

Memantine is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Headache: mild to moderate pain in the head region.
  • Constipation: reduced bowel movements or hard stools.
  • Confusion: transient disorientation or difficulty concentrating.
  • Hypertension: elevated blood pressure readings.
  • Somnolence: increased sleepiness or fatigue.

Serious or Rare Side Effects

  • Seizures: convulsive episodes requiring immediate medical attention.
  • Allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Hallucinations: visual or auditory disturbances.
  • Cardiac arrhythmia: irregular heart rhythm.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

  • Before initiating therapy, consider the following safety measures.
  • 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 reduce risk of additive CNS effects.
  • History of seizures: monitor closely for increased seizure activity.
  • Pregnancy and lactation: safety not established; weigh benefits against potential risks.
  • Store at below 25°C: keep in the original packaging, 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 can increase neuropsychiatric side effects.
  • Cimetidine: may raise memantine plasma concentrations, enhancing toxicity.

Moderate Interactions (Monitor Closely)

  • CNS depressants (e.g., benzodiazepines, alcohol): may augment dizziness or somnolence.
  • Anticholinergic agents: could diminish therapeutic benefit on cognition.
  • Antihypertensive drugs: monitor blood pressure for additive hypotensive effects.

Frequently Asked Questions

Memantine Sandoz contains memantine hydrochloride and is prescribed to treat the cognitive symptoms of mild to moderate Alzheimer’s disease, helping to improve memory, thinking, and daily functioning.

Memantine acts as a non‑competitive antagonist at the NMDA receptor, reducing excessive calcium influx caused by glutamate over‑activation. This protects neurons from excitotoxic damage and supports synaptic activity.

The specific dose and titration schedule are determined by the prescribing clinician based on the patient’s condition, renal function, and tolerability. Patients should follow the prescriber’s instructions precisely.

Safety data for memantine 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 must be made by a healthcare professional.

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 import documentation.

Memantine belongs to the NMDA‑receptor antagonist class, whereas drugs like donepezil are acetylcholinesterase inhibitors. Memantine is typically used for moderate disease and may be combined with an acetylcholinesterase inhibitor for additive benefit.

Store the tablets at temperatures below 25 °C, in the original container, protected from moisture and direct sunlight. Keep out of reach of children and do not use after the expiry date.

Memantine Sandoz is taken orally, usually once daily after a gradual titration period. Tablets should be swallowed whole with water and not crushed or chewed unless otherwise directed by a healthcare professional.

Serious risks include seizures, severe allergic reactions such as anaphylaxis, hallucinations, and cardiac arrhythmias. Patients should seek immediate medical attention if any of these symptoms occur.

Memantine is contraindicated in patients with known hypersensitivity to memantine or any component of the formulation, and it should be used with caution in individuals with severe renal impairment or uncontrolled epilepsy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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