Urantak Tablet (Ranitidine Hydrochloride)
Ranitidine Hydrochloride 168mg
Tablet · Prescription medication
Hanin Pharmaceutical Co., Ltd.
MFDS item code 198600661 · Notified 1986.06.12
This product's status changed to Expired on 2025.04.01. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Improvement of gastric ulcers and gastric mucosal lesions and relief of excessive gastric acid
This medication is effective not only for the treatment of gastric and duodenal ulcers, but also for Zollinger-Ellison syndrome and gastroesophageal reflux disease. It is used for the prevention of postoperative ulcers and for the prevention of gastric ulcers due to NSAID use. It also helps improve gastric mucosal damage such as acute and chronic gastritis flare-ups and upper gastrointestinal bleeding. It is effective for symptoms of excessive gastric acid such as heartburn and regurgitation. Overall, it is used to protect the gastric mucosa and improve symptoms through gastric acid suppression.
As ranitidine, the adult dose is 150 mg once, twice a day, orally in the morning and at bedtime. - For gastric and duodenal ulcers: take 150 mg once, twice a day or 300 mg once, at bedtime. - For duodenal ulcer patients: Take 300 mg once, twice a day, in the morning and at bedtime. - For maintenance therapy of recurrent ulcers: take 150 mg once, at bedtime. - For gastroesophageal reflux disease: 8
For children aged 8 to 18 years, a single dose of 150 mg (2 mg per kg of body weight) may be administered up to twice a day.
This drug should not be used in patients with a history of hypersensitivity to its components. It should also not be administered to patients with a history of acute porphyria, as it may induce acute porphyric attacks. Patients with impaired renal function should use this drug with caution, as it may accumulate in the body; dosage reduction or prolonged dosing intervals may be necessary. Patients with impaired liver function should also use it cautiously. Patients with a history of allergic reactions to medications, elderly patients, and those taking non-steroidal anti-inflammatory drugs should be monitored closely. This drug may mask symptoms of gastric cancer, therefore patients with gastric ulcers or those over middle age with newly occurring dyspeptic symptoms must confirm that it is not a malignant condition before administration. Patients with positive Helicobacter pylori for gastric or duodenal ulcers require eradication therapy. Rarely, allergic reactions or shock symptoms may occur during this medication; if any abnormal symptoms occur, administration should be stopped immediately and medical staff should be consulted. Routine monitoring of blood, liver, and kidney functions is required. Dizziness or drowsiness may occur, so patients should avoid driving or operating dangerous machinery when these symptoms are present. Potential interactions with other medications may occur, so patients should inform the medical staff of any concomitant medications. Pregnant or nursing women should only take this medication when the benefit of treatment outweighs the risks, as its safety has not been established. Safety in children has not been adequately verified, hence caution is required. Elderly patients may require dosage adjustment due to prolonged retention of the drug in the body from renal function decline. Although special intoxication symptoms are rare in cases of overdose, appropriate treatment such as vomiting or gastric lavage may be necessary. This medication should be kept out of the reach of children, and transferring to other containers should be avoided. Long-term use may affect eye health; therefore, regular ophthalmic examinations are recommended.
Shock (anaphylactic shock), urticaria, severe swelling (such as angioedema), tightness in the chest, difficulty breathing, cold sweat, paleness, vascular swelling, severe allergic reactions, jaundice, hepatitis, acute pancreatitis, seizures, consciousness disturbances, myoclonus, severe neurological symptoms, agranulocytosis, pancytopenia, aplastic anemia, acquired immune hemolytic anemia, Stevens-Johnson syndrome, toxic epidermal necrolysis (Lyell syndrome), acute
Urticaria, angioedema, rash, fever, bronchospasm, hypotension, chest pain, granulocytopenia, increased serum creatinine levels, leukopenia, thrombocytopenia, transient and reversible liver function disorders, bradycardia, atrioventricular block, tachycardia, vasculitis, constipation, nausea, vomiting, abdominal distension, abdominal pain, loss of appetite, diarrhea, dizziness, drowsiness, headache, heaviness in the head, insomnia, agitation, anxiety, confusion, depression, hallucinations, blurred vision, involuntary movements
Not everyone experiences these, and they can vary from person to person.
This medication is sensitive to light and should be stored in a light-blocking container. Additionally, it is best stored at room temperature between 1 degree and 30 degrees Celsius. This helps maintain the medication's efficacy.
White, round tablets with a film coating
100 tablets (10 tablets/PTP × 10), 300 tablets/bottle
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.