| Drug Name |
ZANTAC 150 |
| Active Ingredient(s) |
RANITIDINE HYDROCHLORIDE |
Form(s) and Strength(s) Available |
TABLET; ORAL:150MCG |
Product Information / Press Release Qualitative and Quantitative Composition ZANTAC 150mg Tablets: white film-coated, circular, biconvex tablets, engraved ZANTAC 150 on one face and GLAXO on the other. Each tablet contains ranitidine 150mg (as the hydrochloride). ZANTAC Tablets are also indicated for:
- the treatment of duodenal ulcer and benign gastric ulcer associated with non-steroidal anti-inflammatory agents.
- the prevention of non-steroidal anti-inflammatory agent (including aspirin) associated duodenal ulcers in patients with a history of duodenal ulceration proven by endoscopy.
- the treatment of post-operative ulcer
- the treatment of chronic episodic dyspepsia, characterised by pain (epigastric or retrosternal) which is related to meals or disturbs sleep but not associated with the above conditions.
- symptom relief in gastro-oesophageal reflux disease
- the treatment of oesophageal reflux disease
- the treatment of Zollinger-Ellison syndrome
ZANTAC Tablets are also indicated for the following conditions where reduction of gastric secretion and acid output is desirable:
- the prophylaxis of upper gastrointestinal haemorrhage from stress ulceration in seriously ill patients.
- the prophylaxis of recurrent haemorrhage in patients with bleeding peptic ulcers.
- before general anaesthesia in patients considered to be at risk of acid aspiration (Mendelson's syndrome), particularly obstetric patients during labour.
CLINICAL PHARMACOLOGY
ZANTAC is a competitive, reversible inhibitor of the action of histamine at the histamine H 2 -receptors, including receptors on the gastric cells. ZANTAC does not lower serum Ca ++ in hypercalcemic states. ZANTAC is not an anticholinergic agent
Manufacturers URL : www.pfizer.com
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