Antacid MAX® is an antacid and antiflatulent containing a combination of Aluminum Hydroxide, Magnesium Hydroxide and Simethicone.

Deflux^? is a preparation of domperidone. It is a dopamine-receptor blocking agent. It is highly effective for the treatment of gastrointestinal motility disordes such as GERD,diabetic gastroparesis, bloating etc. Its action on the dopamine-receptors in the chemo-emetic trigger zone produces an anti-emetic effect. Therfore, it also highly effective for the treatment of nause, vomiting too.

Flatameal^? DS is an antacid and antiflatulent containing a combination of Aluminium Hydroxide Gel USP, Magnesium Hydroxide BP and Simethicone USP. It is indicated for dyspepsia, hyperacidity, gastric and duodenal ulcer, gastrititis; also for the relief of flatulence, abdominal distention and windy colic.

Frelax^? is a white powder for reconstitution. Polyethylene Glycol 3350 USNF powder for solution is a synthetic polyglycol having an average molecular weight of 3350. Below 55?C it is a free flowing white powder freely soluble in water. It is an osmotic agent for the treatment of constipation. It appears to have no effect on the active absorption or secretion of glucose or electrolytes.It is indicated for the treatment of constipation. This product should be used for two weeks or as directed by the physician.

Lactameal^? is an antacid containing a combination of Aluminium hydroxide B.P as gel) and Magnesium Hydroixde B.P. It is indicated in hyperacidity, gastric ulcer duodenal ulcer and gastritis.

Neoceptin^? R is a histamine H2 receptor antagonist. It inhibits basal and stimulated secretion of gastric acid. It is indicated for the treatment of duodenal ulcer, benign gastric ulcer, post-operative ulcer, reflux oesophagitis, Zollinger Ellison syndrome and in other conditions where reduction of gastric acidity is beneficial. Neoceptin^? R is rapidly absorbed after oral administration. Food or antacid does not interfere its absorption.

Xerod (Tegaserod) is a 5-HT4 receptor partial agonist that binds with high affinity at human 5-HT4 receptors, whereas it has no appreciable affinity for 5-HT3 or dopamine receptors. It has moderate affinity for 5-HT1 receptors. Tegaserod, by acting as an agonist at neuronal 5-HT4 receptors, triggers the release of further neurotransmitters such as calcitonin gene-related peptide from sensory neurons. The activation of 5-HT4 receptors in the gastrointestinal tract stimulates the peristaltic reflex and intestinal secretion, as well as inhibits visceral sensitivity. In vivo studies showed that tegaserod enhanced basal motor activity and normalized impaired motility throughout the gastrointestinal tract. Tegaserod Maleate is indicated for the short-term treatment of irritable bowel syndrom (IBS) whose primary bowel symptom is constipation.

Neokit^? is recommended therapeutic regimens for eradication of Helicobacter pylori in peptic ulcer patients who are positive, include a combination of triple drugs, which are - a proton pump inhibitor (Omeprazole) and two antibiotics (Clarithromycin and Metronidazole). Neokit^? is indicated for eradication of H. pylori in active chronic gastritis, duodenal and gastric ulcers.

Opton^? is a S-isomer of omeprazole.It is a specific inhibitor of the acid pump in the parietal cell.Opton^? is indicated for the healing of erosive esophagitis,long term management of esophagitis, symptomatic GERD & in combination with antibacterials for the treatment of duodenal ulcer associated with H.pylori.Dosage schedule is 20 or 40 mg once daily for 4 to 8 weeks.

Pantobex^? contains Pantoprazole in delayed release tablet form. Pantoprazole is chemically a novel substituted benzimidazole derivative, which suppresses the final step in gastric acid production by forming a covalent bond to two sites of H+-K+ATPase system at the secretory surface of the gastric parietal cell. This leads to inhibition of both basal and stimulated gastric effect that persists longer than 24 hours. Pantoprazole is quantitavely absorbed and its bioavailability does not change up on multiple dosing. Pantobex^? is indicated in the Peptic ulcer diseases, Gastroesophageal reflux diseases(GERD), ulcers induced by the NSAIDs.

Proceptin^? contains omeprazole that belongs to the group of Proton Pump Inhibitor. Proceptin^? works by reducing the amount of acid in the stomach. Proceptin^? is mostly used to: treat stomach and duodenal ulcer disease (also known as peptic ulcer), stop these ulcers from coming back, treat reflux oesophagitis (also known as reflux). These problems are caused, in part, by too much acid in the stomach. This can lead to pain such as heartburn. Proceptin^? is also used to treat Zollinger-Ellison disease.The Food and Drug Administration (FDA) has approved Omeprazole, the first over-the-counter treatment for frequent heartburn.

Protolan^? is a proton pump inhibitor. It is an irreversible inhibitor of the parietal cell H+-K+ATPase, which leads to profound inhibition of gastric acid secretion. It is indicated in Duodenal ulcer,Gastric ulcer, Esophagitis/Ulceration, Zollinger-Ellison syndrome, Resistant ulcers and esophagitis, Eradication of Helicobacter pylori in the treatment of peptic ulcer ( in combinationwith antibiotics)

Pylopac^? is recommended therapeutic regimens for eradication of Helicobacter pylori in peptic ulcer patients who are positive, include a combination of triple drugs, which are - a proton pump inhibitor (Lansoprazole) and two antibiotics (Clarithromycin and Metronidazole). Pylopac^? is indicated for eradication of H. pylori in active chronic gastritis, duodenal and gastric ulcers.

Rostil^? is an musculotropic antispasmodic agent containing Mebeverine Hydrochloride BP. It acts directly on smooth muscle of gastrointestinal tract & used to treat bowel spasm.Rostil^? is indicated for the symptomatic relief of irritable bowel syndrome other conditions include chronic irritable colon, spastic constipation, mucous colitis , colicky abdominal pain and cramps, persistent non-specific diarrhoea.

Serelose^? is a brand of Lactulose, a hyperosmolar laxative - an effective treatment approach for constipation. It is a non-absorbable disaccharide which draws water into the bowel from other body tissues; causes distention through fluid accumulation, thus promotes soft stool and accelerates bowel motion. Serelose^? is indicated for the treatment of mainly constipation. Besides it is indicated in hepatic encephalopathy.Serelose^? is safe in the long term and has been used effectively even in frail elderly patients.

Spanil^? is a preparation of Hyoscine-N-Butylbromide. It is used in symptomatic relief of gastro-intestinal or genito-urinary disorders characterised by smooth muscle spasm.

Taverin^? is a potent synthetic antispasmodic which acts directly on the smooth muscle fibres. Taverin^? has rapid onset of action. In addition to its spasmolytic and vasodialatory actions, Taverin^? elicits a selective blockade of cardiac ? receptors. Taverin^? is indicated in spastic conditions of the gastrointestinal tract like irritable bowel syndrome and biliary colics. It is also indicated in renal colics and spastic conditions of the urogenital tract: nephrolithiasis,ureterolithiasis,pyelitis,cystitis.Moreover Taverin^? is indicated in dysmenorrhoea, imminent abortion and uterine. Taverin^? is of outstanding value in the treatment of coronary insufficiency and angina pectoris owing to its freedom from cardio toxic and hypotensive effects.

Xerod^? (Tegaserod) is a 5-HT4 receptor partial agonist that binds with high affinity at human 5-HT4 receptors, whereas it has no appreciable affinity for 5-HT3 or dopamine receptors. It has moderate affinity for 5-HT1 receptors. Tegaserod, by acting as an agonist at neuronal 5-HT4 receptors, triggers the release of further neurotransmitters such as calcitonin gene-related peptide from sensory neurons. The activation of 5-HT4 receptors in the gastrointestinal tract stimulates the peristaltic reflex and intestinal secretion, as well as inhibits visceral sensitivity. In vivo studies showed that tegaserod enhanced basal motor activity and normalized impaired motility throughout the gastrointestinal tract. Tegaserod Maleate is indicated for the short-term treatment of irritable bowel syndrom (IBS) whose primary bowel symptom is constipation.

The active ingredient of Yamadin^?-20 and Yamadin^?-40 tablet is Famotidine. Famotidine is a novel, highly specific and potent competitive H2- receptor antagonist. It has a rapid onset and prolonged duration of action. Famotidine reduces the acid and pepsin content, as well as the volume of basal, nocturnal and stimulated gastric secretion. Yamadin^? tablet is indicated in short term treatment of active duodenal ulcer and benign gastric ulcer, maintenance therapy for prevention of relapses of duodenal ulceration, gastro-oesophageal reflux disease and Zollinger-Ellison Syndrome.

Zymet^? is a preparation of mammalian pancreas containing enzyme protease, lipase and amylase activity. It is indicated in chldren with reduced or absence of pancreatin exocrine secretion or with cistic fibrosis. It can also be used in adults in conditions with deficient pancreatic exocrine function. The usual dose is 1-3 tablets daily with meal or as directed by the physician.