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Nu-Ranit Tab 150mg: Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx) Current status: Cancelled Post Market
Strength:
150 mg, 300 mg
ATC code:

Patient Medication Information: uses, side effects, how to take - Nu-Ranit Tab 150mg

ABOUT THIS MEDICATION

What the medication is used for:

NU-RANIT, also known as ranitidine hydrochloride is used to treat stomach or intestinal ulcers and prevent their return. It can relieve discomfort from ulcer pain and the heartburn associated with acid reflux.

What it does:

NU-RANIT belongs to a group of medicines called H2-receptor site antagonists. It acts by blocking histamine receptors that are present on the cells in the stomach lining thereby reducing the amount of acid produced by these cells.

When it should not be used:

Do not take NU-RANIT if you have previously had an allergic reaction to the medicine or any of the non-medicinal ingredients of the product.

What the medicinal ingredient is:

Ranitidine Hydrochloride

What the important non-medicinal ingredients are:

Microcrystalline cellulose, hydroxypropyl methylcellulose, polydextrose, titanium dioxide, magnesium stearate, colloidal silicon dioxide, vanillin and carnauba wax.

What dosage forms it comes in:

Tablets, 150 mg and 300 mg

WARNINGS AND PRECAUTIONS

Before you use NU-RANIT talk to your doctor or pharmacist if:

  • you have severe decreased renal function
  • you have lung disease, diabetes or a compromised immune

    system.

  • you are pregnant or breast-feeding.

  • you are older than 65 years of age, for your doctor to rule

    out the possibility of stomach cancer. Also, make sure your doctor knows if you are taking non-steroidal anti-inflammatory drugs (NSAIDs).

  • occurrence of a gastric ulcer is suspected . NU-RANIT can

    mask the symptoms of stomach cancer and therefore delay the diagnosis of this condition.

    This medicine should not be used if you have acute porphyria (a rare blood disorder).

    Experience with NU-RANIT in children below 8 years of age is limited.

INTERACTIONS WITH THIS MEDICATION

Drugs that may interact with this medicine:

  • Non-steroidal anti-inflammatory drugs
  • Ketoconazole
  • Hypoglycemic drugs
  • Theophylline
  • Sucralfate

If you have any concerns regarding drug interactions please consult your pharmacist or physician.

PROPER USE OF THIS MEDICATION

Usual Dose: Duodenal and benign gastric ulcer: 300 mg once daily at bedtime or 150 mg twice daily. In duodenal ulcers, when more rapid healing is desired: 300mg twice daily for 4 weeks.

Maintenance treatment: Duodenal and benign gastric ulcer: 150 mg once daily at bedtime. Duodenal ulcer (smoker): 300 mg nightly. Reflux esophagitis: 300 mg once daily at bedtime or 150 mg twice daily for up to 8 weeks. In patients with moderate to severe esophagitis, may increase to 150 mg four times daily.

Post-operative peptic ulcer: 150 mg twice daily.

Zollinger-Ellison Syndrome: Initially 150 mg three times daily. Some patients may require more frequent dosing.

NSAID-induced lesions (both ulcers and erosions) and their gastrointestinal symptoms and prevention of their recurrence: 150 mg twice daily while continuing NSAID therapy.

Prophylaxis of Acid Aspiration Syndrome: 150 mg the evening prior to anesthesia or 2 hours prior to anesthesia.

Prophylaxis of hemorrhage from stress ulceration or prophylaxis of recurrent hemorrhage from bleeding peptic ulcers: 150mg twice daily for patients on oral feeding.

Elderly patients should start at the lowest recommended dose and be adjusted as necessary.

Overdose:

If you take more than the prescribed dose please consult your physician or Emergency room as soon as possible. SIDE EFFECTS AND WHAT TO DO ABOUT THEM

Like other medications, NU-RANIT can cause some side effects.

Page 25 of 25 These side effects are most likely to be minor and temporary.

Do not be alarmed by this list of possible side effects. You may not experience any of them. If any of these side effects are experienced, do not hesitate to report them to your doctor.

This is not a complete list of side effects. For any unexpected effects while taking NU-RANIT, contact your doctor or pharmacist.

HOW TO STORE IT

Store between 15-30ºC (59-86ºF). Protect from light.

REPORTING SUSPECTED SIDE EFFECTS

To monitor drug safety, Health Canada collects information on serious and unexpected effects of drugs. If you suspect you have had a serious or unexpected reaction to this drug you may notify Health Canada by:

toll-free telephone: 866-234-2345

toll-free fax 866-678-6789

By email: cadrmp@hc-sc.gc.ca

By regular mail:

Canadian Adverse Drug Reaction Monitoring Program (CADRMP)

Health Canada

Address Locator: 0201C2

Ottawa, ON K1A 1B9

NOTE: Before contacting Health Canada, you should contact your physician or pharmacist.

MORE INFORMATION

For more information, please contact your pharmacist, doctor or other healthcare professional or the Dispedia Drug Information Department at: 1-800-667-4708 or visit our website at www.dispedia.com

Date of Revision: January 27, 2009

SERIOUS SIDE EFFECTS, HOW OFTEN THEY HAPPEN
AND WHAT TO DO ABOUT THEM
Symptom / effect

Talk with your

doctor or pharmacist

Stop

taking drug and call your doctor or pharmacist

Only if

severe

In all cases

Headache

Diarrhea

Nausea/vomiting

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Dizziness

Sleepiness or lack of sleep

Vertigo

Blurred vision

Changes to heart rate (increase & decrease) and rhythm

Constipation

Abdominal

discomfort/pain

Pain in the muscles and joints

Tenderness/ soreness of the breasts in males

Skin rash, redness of the skin or hair loss

Allergic reactions

(including chest pain, coughing, fever, rash, swelling, hives, and low blood pressure)

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About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 00865737

Revision date stated in the text: January 27, 2009

Found a mistake? Write to us via the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Nu-Ranit Tab 150mg

Rx or OTC
Prescription (Rx)?
DIN 00865737, 00865745
Schedule(s) PRESCRIPTION
Active ingredient(s) Ranitidine (ranitidine hydrochloride)
Dosage form(s) Tablet
Route(s) of administration Oral
Drug class (WHO ATC)
  1. A Alimentary tract and metabolism drugs
    1. A02 Drugs for acid related disorders
      1. A02B Drugs for peptic ulcer and gastro-oesophageal reflux disease (GORD)
        1. A02BA Histamine H2 receptor antagonists for peptic ulcer and GORD
          1. A02BA02 Ranitidine
Company NU-PHARM INC
Current status Cancelled Post Market
Current status date September 4, 2012
Strengths and forms
DIN Strength Dosage form(s) Current status
00865737 150 MG Tablet Cancelled Post Market September 4, 2012
00865745 300 MG Tablet Cancelled Post Market September 4, 2012

Source: Health Canada – Drug Product Database (DPD) and product monographs, data as of November 1, 2026. Data from the Health Canada Drug Product Database, as published there. Not a substitute for the advice of a doctor or pharmacist.