Product image of Memantine Hydrochloride Activase Pharmaceuticals (Memantine Hydrochloride) supplied by GNH India

Memantine Hydrochloride Activase Pharmaceuticals

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantine Hydrochloride Activase Pharmaceuticals (Memantine Hydrochloride)

Memantine Hydrochloride, the active ingredient in Memantine Hydrochloride Activase Pharmaceuticals, is an NMDA receptor antagonist presented as an oral tablet for oral use. It is indicated for the treatment of Alzheimer’s disease in adult patients.
GNH India supplies Memantine Hydrochloride Activase Pharmaceuticals as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Activase Pharmaceuticals Limited

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Indications & Clinical Uses

  • Memantine Hydrochloride is used in the management of Alzheimer’s disease, a neurodegenerative disorder affecting cognition and daily function.
  • Alzheimer's disease: helps maintain cognitive function and daily living abilities in patients with mild‑to‑moderate or moderate‑to‑severe disease.

How It Works

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

Side Effects

Memantine Hydrochloride may cause a range of adverse reactions. Most are mild and reversible.

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.
  • Fatigue: feeling unusually tired or weak.
  • Confusion: transient difficulty concentrating.
  • Hypertension: elevated blood pressure readings.

Serious or Rare Side Effects

  • Seizures: uncontrolled convulsive episodes.
  • Hallucinations: visual or auditory disturbances.
  • Cardiac arrhythmia: irregular heart rhythm.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Suicidal thoughts: emergence of depressive ideation.
  • Hepatic injury: abnormal liver function tests.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for potential complications.

  • Renal impairment: adjust dose or avoid use in severe dysfunction.
  • History of seizures: monitor closely for increased seizure activity.
  • Cardiovascular disease: observe blood pressure and heart rhythm.
  • Concurrent NMDA antagonists: avoid combined use to reduce neurotoxicity risk.
  • Pregnancy and breastfeeding: safety not established; use only if benefit outweighs risk.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Memantine may interact with other medications that affect the central nervous system or share similar pathways.

Major Interactions (Avoid)

  • Amantadine: additive NMDA antagonism may increase neurotoxicity.
  • Ketamine: combined CNS depression and potential respiratory depression.
  • Other NMDA antagonists: risk of excessive blockade.

Moderate Interactions (Monitor Closely)

  • Anticholinergics: may diminish therapeutic benefit.
  • Diuretics: possible enhancement of hypotensive effects.
  • CNS depressants (e.g., benzodiazepines): monitor for increased sedation.

Frequently Asked Questions

Memantine Hydrochloride Activase is prescribed for the symptomatic treatment of Alzheimer’s disease. It helps to improve or stabilize cognition, memory, and daily functional abilities in adults with mild‑to‑moderate or moderate‑to‑severe disease, as part of a comprehensive care plan.

Memantine works by binding to the NMDA‑type glutamate receptor channel as a non‑competitive antagonist. This blocks excessive calcium entry that occurs during pathological glutamate stimulation, thereby reducing excitotoxic neuronal damage that contributes to cognitive decline in Alzheimer’s disease.

The appropriate dose is determined by the prescribing clinician based on the patient’s age, renal function, and disease severity. Typically, treatment starts with a low dose that is gradually increased, but exact dosing regimens should be obtained from a qualified healthcare professional.

Safety data for Memantine 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 this decision must be made by a qualified healthcare provider.

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 (including any cold‑chain requirements), and necessary import documentation.

The primary alternative class is acetylcholinesterase inhibitors such as donepezil. While those agents increase acetylcholine levels, Memantine reduces glutamate‑mediated excitotoxicity. Clinicians may use them together for complementary mechanisms, but the choice depends on disease stage, tolerability, and individual patient response.

Store the tablets at room temperature, below 25 °C, in the original blister pack or container. Protect them from moisture, excessive heat, and direct sunlight. Keep out of reach of children and do not use if the packaging is damaged.

Memantine is taken orally, usually with or without food, as a tablet. The patient should swallow the tablet whole with water and follow the dosing schedule prescribed by the healthcare professional.

Serious adverse events include seizures, hallucinations, severe skin reactions such as Stevens‑Johnson syndrome, cardiac arrhythmias, and hepatic injury. Any sudden or severe symptoms should prompt immediate medical evaluation.

Memantine is contraindicated in patients with known hypersensitivity to the drug, severe renal impairment where dose adjustment is not feasible, and in individuals taking other NMDA‑receptor antagonists that could cause additive toxicity. Clinicians should assess each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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