Uritin Tablet (Ranitidine Hydrochloride)
Ranitidine Hydrochloride 168mg
Tablet · Prescription medication
Optus Pharmaceutical Co., Ltd.
MFDS item code 201505705 · Approved 2015.08.13
This product's status changed to Expired on 2025.08.13. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Improvement of gastric ulcers and gastric mucosal lesions, relief of symptoms of excessive gastric acid
This medication is effective for various conditions associated with gastric acid, including gastric and duodenal ulcers, Zollinger-Ellison syndrome, and gastroesophageal reflux disease. It is also used to prevent ulcers after surgery and gastric/duodenal ulcers caused by non-steroidal anti-inflammatory drug use. It helps improve damage to the gastric mucosa (erosions, bleeding, redness, swelling) during acute exacerbations of acute and chronic gastritis and is beneficial for treating upper gastrointestinal bleeding. This medication is effective in alleviating symptoms of heartburn and acid regurgitation due to excessive gastric acid. It is used in the treatment and symptom improvement of various gastrointestinal disorders.
As ranitidine, the typical dosage is 150 mg taken orally twice a day, in the morning and at bedtime. For the treatment of gastric and duodenal ulcers: administer 150 mg orally twice daily or 300 mg once daily at bedtime. Patients with duodenal ulcers may take 300 mg orally twice daily in the morning and at bedtime. For the prevention of ulcers induced by non-steroidal anti-inflammatory drugs, the same method of administration as above should be followed.
For children aged 8-18 years, a single dose of 150 mg (2 mg per kg of body weight) may be administered up to twice a day.
This medication should not be used in patients with hypersensitivity to any of the components of this medication. Also, it should not be administered to patients with a history of acute porphyria, as it may trigger acute attacks. In patients with reduced kidney function, the serum concentration of this drug may increase, so adjustment of dose or dosing interval is necessary. Patients with poor liver function should also use this drug cautiously. Patients with a history of hypersensitivity, older adults, and those taking non-steroidal anti-inflammatory drugs should be administered this drug carefully. Especially, since it may mask symptoms of gastric cancer, patients with gastric ulcers or middle-aged persons with recent dyspepsia should confirm malignancy before treatment. Patients with positive Helicobacter pylori gastric and duodenal ulcers require treatment to eradicate the bacteria. This medication may rarely cause hypersensitivity reactions such as anaphylactic shock, hives, angioedema, and rashes, and if any abnormal symptoms occur, usage should be discontinued immediately. Blood-related side effects such as agranulocytosis, leukopenia, and thrombocytopenia may rarely occur, so if symptoms such as fatigue, bleeding, or fever arise, a blood test should be performed. Liver dysfunction may occur, so if jaundice or elevated liver enzyme symptoms develop, treatment should be stopped. Cardiovascular symptoms such as arrhythmias, constipation, nausea, vomiting, abdominal pain, dizziness, drowsiness, and confusion may also occur rarely, so monitoring is necessary. Long-term use of this drug or its use in older adults, patients with chronic lung diseases, or diabetes may increase the risk of pneumonia, so caution is advised. If dizziness or drowsiness occurs, avoid driving or operating dangerous machinery. This medication can interact with other drugs, so particularly when taking anticoagulants, careful monitoring of blood coagulation status is required. Additionally, taking it with sucralfate may reduce absorption; thus, it is advisable to take them with at least a 2-hour interval. Women who are pregnant or may become pregnant, and breastfeeding women, should use this medication cautiously, only when necessary. Safety in children has not been sufficiently confirmed, so caution is needed in its use. Older adults may likely have decreased kidney function, necessitating dose adjustment. Regular blood tests and liver function tests are recommended while taking this medication, as well as kidney function tests. In case of overdose, treatment such as vomiting, gastric lavage, and possibly blood dialysis may be required. Keep this medication out of the reach of children and do not transfer it to another container for safety. This drug may reduce gastric acid secretion and promote bacterial growth in the gastrointestinal tract, so regular examinations including ophthalmological checks are necessary with long-term use.
Rash, fever, hypotension, angioedema, agranulocytosis, elevated serum creatinine, leukopenia, thrombocytopenia, bone marrow suppression, aplastic anemia, hypereosinophilia, hepatic dysfunction (elevated AST, ALT, γ-GTP, ALP), bradycardia, heart block, tachycardia, vasculitis, constipation, nausea, vomiting, abdominal distension, abdominal pain, loss of appetite, diarrhea, dizziness, drowsiness, headache, feeling of heaviness, insomnia, excitement,
Not everyone experiences these, and they can vary from person to person.
This medication may be sensitive to light, so it should be stored in a container that blocks light. Additionally, to keep the medication safe, it is important to store it at room temperature, that is, between 1 degree and 30 degrees Celsius.
White round film-coated tablet
30 tablets/bottle, 300 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
Ranitidine Hydrochloride 168mg
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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.