Viewing nowHwanin Memantin Orally Disintegrating Tablet 20 mg (Memantine Hydrochloride)
Memantine Hydrochloride 20mg
Orally disintegrating Tablet · Prescription medication
Hwanin Pharmaceutical Co., Ltd.

MFDS item code 202400958 · Approved 2024.04.24
Treatment of moderate to severe Alzheimer's disease
This medication is used for the treatment of moderate to severe Alzheimer's disease.
This medication is taken orally once daily, at the same time each day. If necessary, it can be administered twice daily. Place the orally disintegrating tablet on the tongue and let it dissolve without taking it with water. The dosage increase is up to a maximum daily dose of 20 mg, and the dose should be increased by 5 mg weekly over the first 3 weeks. First week (Days 1-7): 5 mg once daily Second week (Days 8-14): 10 mg once daily Third week (Days 15-21): 15 mg once daily Fourth week and onward: 20 mg once daily.
This medication contains the artificial sweetener aspartame, which breaks down into phenylalanine in the body. Therefore, patients with the hereditary condition phenylketonuria should not take this medication. The daily intake of aspartame should be adjusted to not exceed 40 mg per kg of body weight, and for adults, a maximum of 2.4 g per day is considered safe. Patients who are hypersensitive to this medication, those with severe liver disease, and those with significantly diminished kidney function should not take this medication. Patients with epilepsy or a history of seizures should use this medication cautiously, and co-administration with certain NMDA antagonists should be avoided due to increased risk of side effects. Additionally, caution is advised in situations where urine acidity may change, in patients with recent myocardial infarction, heart failure, or uncontrolled hypertension. Side effects may include dizziness, headache, constipation, drowsiness, and hypertension, and psychiatric symptoms or seizures may occur in some patients. There may be interactions with other medications, so consultation with a doctor or pharmacist is required, especially when taking NMDA antagonists, antipsychotics, skeletal muscle relaxants, or anticoagulants. Women who are pregnant or may become pregnant should make a careful decision about taking this medication, as it may pose risks to the fetus, and breastfeeding women are advised to discontinue breastfeeding while using this medication. Safety and efficacy have not been established in children and adolescents under 18 years old, so it is advisable not to use it in this population. In case of overdose, severe symptoms such as coma, hallucinations, and seizures may occur, requiring immediate medical treatment, and since there is no specific antidote, symptomatic treatment is necessary. Finally, this medication may affect a patient's reaction time and concentration, so caution should be exercised while driving or operating machinery, and it should be stored out of reach of children and not transferred to other containers.
Not everyone experiences these, and they can vary from person to person.
This medication may be sensitive to air and moisture, so it should be stored in a tightly closed container. Additionally, avoid extremely hot or cold places, and store at room temperature between 1 and 30 degrees Celsius.
White round orally disintegrating tablet
90 tablets/box [(10 tablets/PTP × 9)]
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.