Product image of Memantine Hydrochloride Milpharm Limited (Memantine Hydrochloride) supplied by GNH India

Memantine Hydrochloride Milpharm Limited

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantine Hydrochloride Milpharm Limited (Memantine Hydrochloride)

Memantine, the active ingredient in Memantine Hydrochloride Milpharm Limited, is an NMDA receptor antagonist presented as an oral tablet for oral use. It treats moderate to severe Alzheimer’s disease in adults.
GNH India supplies Memantine Hydrochloride Milpharm Limited as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Milpharm Limited

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Indications & Clinical Uses

Memantine is used in the management of Alzheimer’s disease, acting on the glutamatergic pathway to support cognitive function.

  • Alzheimer’s disease (moderate to severe): improves cognition and daily functioning in patients with advanced disease.
  • Alzheimer’s disease (mild to moderate): may be used as adjunct therapy together with cholinesterase inhibitors.
  • Behavioral symptoms of Alzheimer’s disease: can help reduce agitation and aggression when prescribed by a physician.

How It Works

  • Memantine acts as a non‑competitive antagonist at the NMDA (N‑methyl‑D‑aspartate) receptor. By binding to the receptor-associated ion channel with moderate affinity, it blocks excessive calcium influx caused by overstimulation with glutamate, thereby reducing excitotoxic neuronal injury that contributes to cognitive decline in Alzheimer’s disease.

Side Effects

Memantine is associated with a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Headache: mild to moderate intensity.
  • Constipation: reduced bowel movements.
  • Fatigue: feeling unusually tired.
  • Nausea: mild stomach upset.
  • Confusion: occasional disorientation.

Serious or Rare Side Effects

  • Seizures: rare occurrence of convulsive episodes.
  • Severe allergic reaction: rash, swelling, or difficulty breathing.
  • Hallucinations: visual or auditory disturbances.
  • Hypertension: sudden increase in blood pressure.

Precautions & Warnings

When prescribing memantine, clinicians should consider several safety aspects.

  • Renal impairment: dose adjustment may be required in patients with reduced kidney function.
  • Hepatic disease: monitor liver enzymes and consider dose modification.
  • Concomitant CNS disorders: use caution in patients with epilepsy or other seizure disorders.
  • Pregnancy and breastfeeding: avoid use unless benefits clearly outweigh potential risks.
  • Elderly patients: start at low dose and titrate slowly to minimize adverse effects.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, and protect from moisture.

Avoid Interactions

Memantine may interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Amantadine: combined NMDA antagonism can increase risk of neuropsychiatric effects.
  • Ketamine: additive NMDA blockade may lead to severe dizziness or confusion.

Moderate Interactions (Monitor Closely)

  • Anticholinesterases (e.g., donepezil): monitor for additive cognitive effects.
  • Diuretics (e.g., furosemide): may increase serum memantine concentrations.
  • Antihypertensives: observe for potential blood pressure changes.

Frequently Asked Questions

Memantine Hydrochloride Milpharm is indicated for the treatment of moderate to severe Alzheimer’s disease. It helps improve cognition, memory, and daily functional abilities in patients with this neurodegenerative condition when prescribed by a qualified healthcare professional.

Memantine works by blocking the NMDA‑type glutamate receptors in a non‑competitive manner. This reduces excessive calcium entry into neurons, limiting excitotoxic damage that contributes to the progressive loss of cognitive function seen in Alzheimer’s disease.

The dosage of memantine is individualized and set by the prescribing clinician based on the patient’s clinical status, renal function, and tolerability. The prescriber determines the appropriate starting dose and titration schedule.

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

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 most other Alzheimer’s agents are cholinesterase inhibitors (e.g., donepezil). Memantine is typically used in moderate to severe stages and can be combined with a cholinesterase inhibitor for additive benefit, while the latter are often started earlier in the disease course.

Memantine tablets should be stored at ambient temperature, below 25 °C. Keep them in the original container, protect from moisture, and store away from direct sunlight to maintain product stability.

Memantine is administered orally, usually as a tablet taken with or without food. The exact dosing schedule, including the number of tablets per day, is determined by the prescribing physician.

Serious risks include the potential for seizures, severe allergic reactions (such as rash or breathing difficulty), and rare neuropsychiatric events like hallucinations. Patients should be monitored for these events, especially during dose escalation.

Memantine is contraindicated in patients with known hypersensitivity to the drug. Caution is advised for individuals with uncontrolled epilepsy, severe renal impairment, or those taking other strong NMDA antagonists, as the risk of adverse effects may be heightened.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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