Pantoprazole 20mg gastro-resistant tablets United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

pantoprazole 20mg gastro-resistant tablets

de pharmaceuticals - pantoprazole sodium sesquihydrate - gastro-resistant tablet - 20mg

Pantoprazole 40mg gastro-resistant tablets United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

pantoprazole 40mg gastro-resistant tablets

de pharmaceuticals - pantoprazole sodium sesquihydrate - gastro-resistant tablet - 40mg

Pantoprazole 20mg Gastro-Resistant Tablets Malta - English - Medicines Authority

pantoprazole 20mg gastro-resistant tablets

aurobindo pharma (malta) limited vault 14, level 2, valletta waterfront, floriana frn 1913, malta - pantoprazole sodium, sesquihydrate - gastro-resistant tablet - pantoprazole sodium sesquihydrate 20 mg - drugs for acid related disorders

Pantoprazole 40mg Gastro-Resistant Tablets Malta - English - Medicines Authority

pantoprazole 40mg gastro-resistant tablets

aurobindo pharma (malta) limited vault 14, level 2, valletta waterfront, floriana frn 1913, malta - pantoprazole sodium, sesquihydrate - gastro-resistant tablet - pantoprazole sodium sesquihydrate 40 mg - drugs for acid related disorders

IPCA PANTOPRAZOLE pantoprazole (as sodium sesquihydrate) 40 mg enteric-coated tablet blister pack. Australia - English - Department of Health (Therapeutic Goods Administration)

ipca pantoprazole pantoprazole (as sodium sesquihydrate) 40 mg enteric-coated tablet blister pack.

ipca pharma (australia) pty ltd - pantoprazole sodium sesquihydrate, quantity: 45.4 mg (equivalent: pantoprazole, qty 40 mg) - tablet, enteric coated - excipient ingredients: mannitol; sodium carbonate; sodium starch glycollate; crospovidone; colloidal anhydrous silica; calcium stearate; hypromellose; macrogol 6000; sodium hydroxide; polysorbate 80; purified water; methacrylic acid copolymer; sodium lauryl sulfate; titanium dioxide; purified talc; iron oxide yellow; xanthan gum; polyvinyl alcohol; lecithin - 1. for symptomatic improvement and healing of gastrointestinal diseases which require a reduction in acid secretion: i) duodenal ulcer; ii) gastric ulcer; iii) gastro-oesophageal reflux disease (gord): symptomatic gord. the treatment of heartburn and other symptoms associated with gord; reflux oesophagitis; iv) gastrointestinal lesions refractory h2 blockers; v) zollinger-ellison syndrome. patients whose gastric or duodenal ulceration is not associated with ingestion of non-steroidal anti-inflammatory drugs (nsaids) require treatment with antimicrobial agents in addition to antisecretory drugs whether on first presentation or on recurrence. 2. maintenance of healed reflux oesophagitis in patients previously treated for moderate to severe reflux oesophagitis. 3. prevention of gastroduodenal lesions and dyspeptic symptoms associated with non-selective non-steroidal anti-inflammatory drugs (nsaids) in increased risk patients with a need for continuous non-selective nsaid treatment.

AG-PANTOPRAZOLE SODIUM TABLET (DELAYED-RELEASE) Canada - English - Health Canada

ag-pantoprazole sodium tablet (delayed-release)

angita pharma inc. - pantoprazole (pantoprazole sodium sesquihydrate) - tablet (delayed-release) - 20mg - pantoprazole (pantoprazole sodium sesquihydrate) 20mg - proton-pump inhibitors

AG-PANTOPRAZOLE SODIUM TABLET (DELAYED-RELEASE) Canada - English - Health Canada

ag-pantoprazole sodium tablet (delayed-release)

angita pharma inc. - pantoprazole (pantoprazole sodium sesquihydrate) - tablet (delayed-release) - 40mg - pantoprazole (pantoprazole sodium sesquihydrate) 40mg - proton-pump inhibitors

NOUMED PANTOPRAZOLE pantoprazole (as sodium sesquihydrate) 40mg enteric coated tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

noumed pantoprazole pantoprazole (as sodium sesquihydrate) 40mg enteric coated tablet blister pack

avallon pharmaceuticals pty ltd - pantoprazole sodium sesquihydrate, quantity: 45.1 mg (equivalent: pantoprazole, qty 40 mg) - tablet, enteric coated - excipient ingredients: hyprolose; calcium stearate; triethyl citrate; crospovidone; sodium carbonate; colloidal anhydrous silica; microcrystalline cellulose; titanium dioxide; hypromellose; iron oxide yellow; quinoline yellow aluminium lake; macrogol 400; brilliant scarlet 4r aluminium lake; polysorbate 80; purified water; methacrylic acid copolymer; sodium lauryl sulfate - 1. for symptomatic improvement and healing of gastrointestinal diseases which require a reduction in acid secretion: duodenal ulcer; gastric ulcer; gastro-oesophageal reflux disease (gord) i. symptomatic gord. the treatment of heartburn and other symptoms associated with gord ii. reflux oesophagitis; gastrointestinal lesions refractory to h2 blockers ; zollinger-ellison syndrome. patients whose gastric or duodenal ulceration is not associated with ingestion of non-steroidal anti-inflammatory drugs (nsaids) require treatment with antimicrobial agents in addition to antisecretory drugs whether on first presentation or on recurrence. 2. maintenance of healed reflux oesophagitis in patients previously treated for moderate to severe reflux oesophagitis. 3. for eradication of helicobacter pylori, treatment with pantoprazole and one of the following combinations of antibiotics: clarithromycin and amoxicillin or; clarithromycin and metronidazole or; amoxicillin and metronidazole - is recommended in cases of duodenal ulcer and gastric ulcer with the objective of reducing the recurrence of duodenal and gastric ulcers caused by this micro-organism. 4. pantoprazole in combination with bismuth, metronidazole and tetracycline is indicated for the eradication of helicobacter pylori associated with peptic ulcer disease with the objective of reducing the recurrence of peptic ulcers caused by this organism. 5. prevention of gastroduodenal lesions and dyspeptic symptoms associated with non-selective non-steroidal anti-inflammatory drugs (nsaids) in increased risk patients with a need for continuous non-selective nsaid treatment.