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

Memantine Hydrochloride Genus

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantine Hydrochloride Genus (Memantine Hydrochloride)

Memantine Hydrochloride, the active ingredient in Memantine Hydrochloride Genus, is an NMDA receptor antagonist presented as a tablet for oral use. It is indicated for the treatment of moderate to severe dementia associated with Alzheimer’s disease in adult patients, helping to preserve cognitive function and daily living abilities.

GNH India supplies Memantine Hydrochloride Genus as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with established quality‑assurance processes and regulatory compliance across European and global markets and reliable distribution networks.

Manufacturer / TM Owner

Genus Pharmaceuticals Limited

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Indications & Clinical Uses

Memantine Hydrochloride is used in the management of neurodegenerative conditions affecting the glutamatergic pathway, primarily Alzheimer’s disease.

  • Alzheimer's disease (moderate to severe): improves cognition and functional abilities in adult patients.
  • Dementia associated with Alzheimer’s disease (moderate to severe): helps maintain daily living activities and slows functional decline.
  • Cognitive decline in Alzheimer’s disease: may provide modest benefit in memory and executive function.

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 with moderate affinity, it reduces excessive calcium influx caused by prolonged glutamate activation. This moderates excitotoxic neuronal injury and stabilises synaptic transmission, while preferentially blocking pathological over‑activation and preserving normal physiological NMDA activity, allowing essential neurotransmission to continue.

Side Effects

Memantine Hydrochloride may be associated with a range of adverse reactions, which are generally classified by frequency and severity.

Common Side Effects

  • Dizziness
  • Headache
  • Constipation
  • Fatigue

Serious or Rare Side Effects

  • Seizures
  • Cardiac arrhythmia
  • Severe allergic reaction (anaphylaxis)

Precautions & Warnings

When prescribing Memantine Hydrochloride, clinicians should consider several safety factors.

  • Renal impairment: dose adjustment may be required; monitor renal function.
  • History of seizures: use with caution and monitor for increased seizure activity.
  • Cardiovascular disease: assess blood pressure and heart rate regularly.
  • Concomitant use with other NMDA antagonists: avoid due to additive neurotoxicity risk.
  • Pregnancy: safety not established; avoid unless benefits outweigh risks.
  • Store at room temperature: keep in original packaging, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Amantadine: combined NMDA antagonism may increase neurotoxicity.
  • Other NMDA receptor antagonists (e.g., ketamine): additive CNS effects.

Moderate Interactions (Monitor Closely)

  • Anticholinesterase inhibitors (donepezil, rivastigmine): monitor for synergistic cognitive effects.
  • Diuretics (e.g., furosemide): may enhance hypotensive effect.
  • CNS depressants (benzodiazepines, alcohol): monitor for increased sedation.
  • Antihypertensive agents: monitor blood pressure.

Frequently Asked Questions

Memantine Hydrochloride Genus is an antidementia agent indicated for moderate to severe Alzheimer’s disease dementia. It helps improve cognitive function and supports daily living activities in adult patients by modulating glutamatergic neurotransmission.

The drug acts as a non‑competitive antagonist at NMDA receptors, reducing excessive calcium influx caused by prolonged glutamate activation. This limits excitotoxic neuronal damage and stabilises synaptic activity, which contributes to its clinical benefit in Alzheimer’s disease.

Dosing is individualized and set by the prescribing clinician based on the patient’s clinical condition, renal function and tolerability. Specific dose regimens are not provided here and should follow the prescriber’s instructions.

Safety data are limited; the product is classified as pregnancy category unknown. It should only be used during pregnancy or lactation if the potential benefit justifies the potential risk to the fetus or infant, and under medical supervision.

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 targets the glutamatergic system as an NMDA receptor antagonist, whereas acetylcholinesterase inhibitors enhance cholinergic transmission. This complementary mechanism allows memantine to be used alone or together with cholinergic agents for moderate to severe disease, offering a different therapeutic approach.

Store the product at room temperature, below 25 °C, in the original container. Keep it protected from moisture and light, and avoid storing in bathrooms or near heat sources.

The medication is taken orally, typically as a tablet, with or without food as directed by the prescriber. Swallow the tablet whole with water and follow the dosing schedule provided by the healthcare professional.

Serious adverse reactions can include seizures, cardiac arrhythmias and severe allergic responses such as anaphylaxis. Patients experiencing any of these symptoms should seek immediate medical attention.

Individuals with known hypersensitivity to memantine or its excipients, those with uncontrolled severe renal impairment, or patients for whom the risk–benefit assessment is unfavorable should avoid using this medication.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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