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Tradename: TRITEC
Summary for Tradename: TRITEC
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Clinical Trials for: TRITECBioequivalency Study of Ranitidine Tablets 300 mg of Dr. Reddy's Under Fasting Conditions Status: Completed Condition: Healthy Study in Healthy Volunteers to Assess Effect of Omeprazole and Ranitidine on the Pharmacokinetics of Vandetanib Status: Completed Condition: Pharmacokinetic; Cmax; Tmax; Plasma AUC; Plasma [AUC(0-t)]; Plasma [AUC(0-672)]; (t1/2,λz) Effect of Ranitidine on Hyper-IgE Recurrent Infection (Job's) Syndrome Status: Terminated Condition: JOB's Syndrome; Hyper-IgE Recurrent Infection Syndrome; Immune Deficiency Comparison of Pantoprazole and Ranitidine in Dyspepsia Status: Recruiting Condition: Dyspepsia Efficacy and Safety Study of Esomeprazole 20mg qd vs Ranitidine 150mg Bid in Patients With an NSAID-induced Gastric Ulcer Status: Completed Condition: Gastric Ulcer A Study To Investigate The Effectiveness Of AH234844 (Lavoltidine) Compared With NEXIUM And Ranitidine. Status: Completed Condition: Gastroesophageal Reflux Disease; Reflux, Gastroesophageal A Study to Evaluate The Effects of Two Different Meal Types, Omeprazole And Ranitidine On Danoprevir Pharmacokinetics When Coadministered With Ritonavir in Healthy Volunteers Status: Completed Condition: Healthy Volunteer A Comparative Efficacy and Safety Study of Nexium Delayed-Release Capsules (40mg qd and 20mg qd) Versus Ranitidine 150mg Bid for the Healing of NSAID-Associated Gastric Ulcers When Daily NSAID Use is Continued Status: Completed Condition: NSAID Associated Gastric Ulcers Effect of Single Doses of YF476 on Stomach Acidity Compared With Ranitidine and Placebo in Fasted and Fed States Status: Completed Condition: Reflux Oesophagitis A Comparative Efficacy and Safety Study of Nexium Delayed-Release Capsules (40mg qd and 20mg qd) Versus Ranitidine 150mg Bid for the Healing of NSAID-Associated Gastric Ulcers When Daily NSAID Use is Continued in Subjects in the US Only Status: Completed Condition: NSAID Associated Gastric Ulcers Courtesy of ClinicalTrials.org See more clinical trials for this drug | ||||||||
Glossary
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Type | RLD | Patent No. | Product | Substance | Delist_Flag | Patent Expiration | Exclusivity Expiration | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Glaxosmithkline | TRITEC | ranitidine bismuth citrate | TABLET; ORAL | 020559 | Aug 8, 1996 | DISCN | No | 5,456,925 | <disabled> | <disabled> | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Glaxosmithkline | TRITEC | ranitidine bismuth citrate | TABLET; ORAL | 020559 | Aug 8, 1996 | DISCN | No | 5,601,848 | <disabled> | <disabled> | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Glaxosmithkline | TRITEC | ranitidine bismuth citrate | TABLET; ORAL | 020559 | Aug 8, 1996 | DISCN | No | 5,629,297 | <disabled> | <disabled> | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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