TEVA-RANITIDINE TABLET Kanada - angielski - Health Canada

teva-ranitidine tablet

teva canada limited - ranitidine (ranitidine hydrochloride) - tablet - 150mg - ranitidine (ranitidine hydrochloride) 150mg - histamine h2-antagonists

TEVA-RANITIDINE INJECTION SOLUTION Kanada - angielski - Health Canada

teva-ranitidine injection solution

teva canada limited - ranitidine (ranitidine hydrochloride) - solution - 25mg - ranitidine (ranitidine hydrochloride) 25mg - histamine h2-antagonists

TEVA-RANITIDINE SOLUTION Kanada - angielski - Health Canada

teva-ranitidine solution

teva canada limited - ranitidine (ranitidine hydrochloride) - solution - 75mg - ranitidine (ranitidine hydrochloride) 75mg - histamine h2-antagonists

RAN-RANITIDINE TABLET Kanada - angielski - Health Canada

ran-ranitidine tablet

ranbaxy pharmaceuticals canada inc. - ranitidine (ranitidine hydrochloride) - tablet - 150mg - ranitidine (ranitidine hydrochloride) 150mg - histamine h2-antagonists

RAN-RANITIDINE TABLET Kanada - angielski - Health Canada

ran-ranitidine tablet

ranbaxy pharmaceuticals canada inc. - ranitidine (ranitidine hydrochloride) - tablet - 300mg - ranitidine (ranitidine hydrochloride) 300mg - histamine h2-antagonists

RANITIDINE- ranitidine hydrochloride tablet Stany Zjednoczone - angielski - NLM (National Library of Medicine)

ranitidine- ranitidine hydrochloride tablet

northwind pharmaceuticals, llc - ranitidine hydrochloride (unii: bk76465ihm) (ranitidine - unii:884kt10yb7) - ranitidine 150 mg - ranitidine tablets, usp is indicated in: 1. short-term treatment of active duodenal ulcer. most patients heal within 4 weeks. studies available to date have not assessed the safety of ranitidine in uncomplicated duodenal ulcer for periods of more than 8 weeks. 2. maintenance therapy for duodenal ulcer patients at reduced dosage after healing of acute ulcers. no placebo-controlled comparative studies have been carried out for periods of longer than 1 year. 3. the treatment of pathological hypersecretory conditions (e.g., zollinger-ellison syndrome and systemic mastocytosis). 4. short-term treatment of active, benign gastric ulcer. most patients heal within 6 weeks and the usefulness of further treatment has not been demonstrated. studies available to date have not assessed the safety of ranitidine in uncomplicated, benign gastric ulcer for periods of more than 6 weeks. 5. maintenance therapy for gastric ulcer patients at reduced dosage after healing of acute ulcers. placebo-controlled studies have been carried

RANITIDINE- ranitidine hydrochloride solution Stany Zjednoczone - angielski - NLM (National Library of Medicine)

ranitidine- ranitidine hydrochloride solution

carilion materials management - ranitidine hydrochloride (unii: bk76465ihm) (ranitidine - unii:884kt10yb7) - ranitidine 15 mg in 1 ml - ranitidine oral solution is indicated in: - short-term treatment of active duodenal ulcer. most patients heal within 4 weeks. studies available to date have not assessed the safety of ranitidine in uncomplicated duodenal ulcer for periods of more than 8 weeks. - maintenance therapy for duodenal ulcer patients at reduced dosage after healing of acute ulcers. no placebo-controlled comparative studies have been carried out for periods of longer than 1 year. - the treatment of pathological hypersecretory conditions (e.g., zollinger-ellison syndrome and systemic mastocytosis). - short-term treatment of active, benign gastric ulcer. most patients heal within 6 weeks and the usefulness of further treatment has not been demonstrated. studies available to date have not assessed the safety of ranitidine in uncomplicated, benign gastric ulcer for periods of more than 6 weeks. - maintenance therapy for gastric ulcer patients at reduced dosage after healing of acute ulcers. placebo-controlled studies have been carried out

Arrow - Ranitidine 150 Nowa Zelandia - angielski - Medsafe (Medicines Safety Authority)

arrow - ranitidine 150

actavis new zealand limited - ranitidine hydrochloride 168mg equivalent to ranitidine 150 mg;   - film coated tablet - 150 mg - active: ranitidine hydrochloride 168mg equivalent to ranitidine 150 mg   excipient: croscarmellose sodium magnesium stearate microcrystalline cellulose opadry white ys-22-18096 purified water

Arrow - Ranitidine 300 Nowa Zelandia - angielski - Medsafe (Medicines Safety Authority)

arrow - ranitidine 300

actavis new zealand limited - ranitidine hydrochloride 336mg equivalent to ranitidine 300 mg;   - film coated tablet - 300 mg - active: ranitidine hydrochloride 336mg equivalent to ranitidine 300 mg   excipient: croscarmellose sodium magnesium stearate microcrystalline cellulose opadry white ys-22-18096 purified water

RANITIDINE- ranitidine tablet Stany Zjednoczone - angielski - NLM (National Library of Medicine)

ranitidine- ranitidine tablet

rebel distributors - ranitidine hydrochloride (unii: bk76465ihm) (ranitidine - unii:884kt10yb7) - ranitidine hydrochloride 150 mg - ranitidine tablets, usp is indicated in: 1. short-term treatment of active duodenal ulcer. most patients heal within 4 weeks. studies available to date have not assessed the safety of ranitidine in uncomplicated duodenal ulcer for periods of more than 8 weeks. 2. maintenance therapy for duodenal ulcer patients at reduced dosage after healing of acute ulcers. no placebo-controlled comparative studies have been carried out for periods of longer than 1 year. 3. the treatment of pathological hypersecretory conditions (e.g., zollinger-ellison syndrome and systemic mastocytosis). 4. short-term treatment of active, benign gastric ulcer. most patients heal within 6 weeks and the usefulness of further treatment has not been demonstrated. studies available to date have not assessed the safety of ranitidine in uncomplicated, benign gastric ulcer for periods of more than 6 weeks. 5. maintenance therapy for gastric ulcer patients at reduced dosage after healing of acute ulcers. placebo-controlled studies have been carried