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

Memantina Aurobindo

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantina Aurobindo (Memantine Hydrochloride)

Memantine Hydrochloride, the active ingredient in Memantina Aurobindo, is a NMDA receptor antagonist presented as an oral formulation for oral use. It is indicated for the treatment of moderate to severe Alzheimer’s disease and dementia associated with Alzheimer’s disease in adult patients.

GNH India supplies Memantina Aurobindo as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Aurobindo Pharma (Italia) S.R.L.

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Indications & Clinical Uses

Memantina Aurobindo is an NMDA‑receptor antagonist used in the management of Alzheimer‑related cognitive disorders.

  • Moderate to severe Alzheimer’s disease: Improves cognition, memory and daily functional abilities.
  • Dementia associated with Alzheimer’s disease: Helps maintain functional independence.
  • Alzheimer’s‑related neuropsychiatric symptoms: May reduce agitation and aggression in some patients.

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 overstimulation, thereby decreasing excitotoxic neuronal damage that contributes to cognitive decline in Alzheimer’s disease.

Side Effects

Memantina Aurobindo may cause a range of adverse reactions, most of which are dose‑related and reversible.

Common Side Effects

  • Dizziness
  • Headache
  • Constipation
  • Fatigue
  • Confusion
  • Hypertension

Serious or Rare Side Effects

  • Seizures
  • Cardiac arrhythmias
  • Hepatic dysfunction
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis
  • Severe hypotension
  • Neuroleptic malignant‑like syndrome

Precautions & Warnings

When prescribing Memantina Aurobindo, clinicians should consider several safety factors.

  • Renal impairment: Monitor renal function and adjust therapy as needed.
  • History of seizures: Evaluate risk and observe for seizure activity.
  • Cardiovascular disease: Monitor blood pressure and heart rhythm regularly.
  • Concomitant NMDA antagonists: Avoid combined use to prevent additive neurotoxicity.
  • Pregnancy and lactation: Safety unknown; use only if potential benefit justifies the risk.
  • Store at room temperature: Keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Memantina Aurobindo can interact with other medicines that affect the central nervous system or cardiovascular system.

Major Interactions (Avoid)

  • Amantadine: Increases risk of CNS adverse effects.
  • Ketamine: Additive NMDA antagonism may lead to excessive neuroinhibition.
  • Other NMDA antagonists: Combined use can cause severe neurotoxicity.

Moderate Interactions (Monitor Closely)

  • Antihypertensive agents: May enhance hypotensive effect.
  • Diuretics: Potential electrolyte disturbances.
  • CNS depressants (e.g., benzodiazepines): May increase sedation and dizziness.

Frequently Asked Questions

Memantina Aurobindo contains memantine hydrochloride and is prescribed for moderate to severe Alzheimer’s disease and dementia associated with Alzheimer’s disease. It helps improve cognition, memory, and daily functioning in adult patients with these conditions.

Memantine acts as a non‑competitive antagonist at NMDA receptors, reducing excessive calcium influx caused by glutamate over‑activation. This limits excitotoxic neuronal injury, which is a key contributor to the cognitive decline seen in Alzheimer’s disease.

The dosage of Memantina Aurobindo is determined by the prescribing physician based on the patient’s clinical condition, renal function, and response to therapy. The prescriber will set the appropriate dose and titration schedule.

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

To place an order, 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 necessary import documentation.

Memantine belongs to the NMDA‑receptor antagonist class, whereas cholinesterase inhibitors such as donepezil act by increasing acetylcholine levels. Memantine is typically used in moderate to severe stages, often in combination with a cholinesterase inhibitor, offering a complementary mechanism of neuroprotection.

Store Memantina Aurobindo at room temperature, below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed to maintain stability.

Memantina Aurobindo is taken orally, usually with or without food, as directed by the prescribing physician. The tablets should be swallowed whole with a glass of water and not chewed or crushed unless specifically instructed.

Serious adverse events, although rare, include seizures, severe hypotension, cardiac arrhythmias, hepatic dysfunction, and severe skin reactions such as Stevens‑Johnson syndrome. Patients should be monitored closely for any of these symptoms and seek immediate medical attention if they occur.

Memantina Aurobindo is contraindicated in patients with known hypersensitivity to memantine or any of its excipients. Caution is advised in individuals with severe renal impairment, uncontrolled hypertension, or a history of seizures, and it should be avoided in combination with other NMDA antagonists.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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