Gastric Ulcer
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Sign up freeTop drugs studied for this disease
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FDA approval · 2009-04-06FDA Approved: RANITIDINE — Supplemental Application (Dr. Reddy's Laboratories Limited)
FDA approved a supplemental application for ranitidine submitted by Dr. Reddy's Laboratories Limited.
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FDA approval · 2009-02-27FDA Approved: CIMETIDINE 200 ACID REDUCER — Supplemental Application (Walgreen Company)
FDA approved a supplemental application to approve Walgreens' Cimetidine 200 Acid Reducer as a generic cimetidine product.
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FDA approval · 2009-01-21FDA Approved: OMEPRAZOLE — Supplemental Application (Quallent Pharmaceuticals Health LLC)
The FDA approved a supplemental application for omeprazole filed by Quallent Pharmaceuticals Health LLC under an ANDA.
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FDA approval · 2009-01-21FDA Approved: OMEPRAZOLE — Original Application (Sandoz Inc)
FDA approved the original application for omeprazole from Sandoz Inc, authorizing a generic version of this proton pump inhibitor.
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FDA approval · 2008-12-01FDA Approved: PRILOSEC — Supplemental Application (Covis Pharma US, Inc)
FDA approved a supplemental application for Prilosec (omeprazole magnesium) by Covis Pharma US, Inc. to update and/or expand the product lab…
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FDA approval · 2008-11-24FDA Approved: ACID CONTROLLER — Supplemental Application (H E B)
FDA approved a supplemental application for ACID CONTROLLER (famotidine) from H E B. The approval expands the product's labeling/indications…
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CLINICAL_TRIALS trial_result · 2008-10-23Clinical Trial Update: Effect of Naproxen, Aspirin, Celecoxib, or Clopidogrel on the Healing of Stomach and Intestinal Ulcers [Phase 4]
A Phase 4 trial evaluating whether naproxen, aspirin, celecoxib, or clopidogrel affect healing of gastric and duodenal ulcers; the study is …
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FDA approval · 2008-09-12FDA Approved: SUCRALFATE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approved a supplemental application for sucralfate by Teva Pharmaceuticals USA, Inc., marking an approved modification to the generic pr…
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FDA approval · 2008-06-30FDA Approved: ACIPHEX — Supplemental Application (Waylis Therapeutics LLC)
The FDA approved a supplemental application for ACIPHEX (rabeprazole sodium) submitted by Waylis Therapeutics LLC.
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FDA approval · 2008-06-25FDA Approved: FAMOTIDINE — Original Application (Mylan Institutional LLC)
The FDA approved a generic famotidine product from Mylan Institutional LLC under an original ANDA.
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FDA approval · 2008-06-03FDA Approved: FAMOTIDINE — Supplemental Application (Sagent Pharmaceuticals)
The FDA approved Sagent Pharmaceuticals' supplemental application for famotidine under an existing ANDA, updating the product's approved lab…
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FDA approval · 2008-06-03FDA Approved: FAMOTIDINE — Supplemental Application (Sagent Pharmaceuticals)
FDA approved a supplemental application for famotidine from Sagent Pharmaceuticals, confirming the generic product under ANDA075651.
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FDA approval · 2008-05-20FDA Approved: FAMOTIDINE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for famotidine (Hikma Pharmaceuticals USA Inc.). The approval updates the labeling to reflect additi…
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FDA approval · 2008-04-21FDA Approved: PREVACID — Supplemental Application (Takeda Pharmaceuticals America, Inc.)
The FDA approved a supplemental application for PREVACID (lansoprazole) filed by Takeda Pharmaceuticals America, Inc.
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FDA approval · 2008-04-21FDA Approved: PREVACID SOLUTAB — Supplemental Application (Takeda Pharmaceuticals America, Inc.)
FDA approves a supplemental application for PREVACID SOLUTAB (lansoprazole) filed by Takeda Pharmaceuticals America, expanding the product's…
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CLINICAL_TRIALS trial_result · 2008-03-24Clinical Trial Update: Dose-Effect of S-Tenatoprazole-Na(STU-Na) 30 mg, 60 mg, 90 mg and 120 mg in Healthy Volunteers [Phase 1]
Phase 1 dose-escalation study of S-Tenatoprazole-Na (30, 60, 90, 120 mg) in healthy volunteers to characterize dose-related pharmacodynamics…
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FDA approval · 2008-02-27FDA Approved: FAMOTIDINE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved a supplemental application for famotidine from Teva Pharmaceuticals USA, Inc., updating the approved generic product.
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FDA approval · 2008-02-06FDA Approved: ACID REDUCER PLUS ANTACID — Original Application (CVS Pharmacy)
FDA approved the original application for ACID REDUCER PLUS ANTACID, a combination product containing famotidine with calcium carbonate and …
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FDA approval · 2007-12-21FDA Approved: OMEPRAZOLE AND SODIUM BICARBONATE — Supplemental Application (Oceanside Pharmaceuticals)
FDA approved a supplemental application for the combination product omeprazole and sodium bicarbonate from Oceanside Pharmaceuticals.
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FDA approval · 2007-12-20FDA Approved: PROTONIX I.V. — Supplemental Application (Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.)
FDA approved a supplemental application to add an intravenous form of pantoprazole (PROTONIX I.V.), expanding the approved route of administ…
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FDA approval · 2007-11-14FDA Approved: PROTONIX DELAYED-RELEASE — Original Application (Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.)
FDA approved the original application for Pantoprazole sodium delayed-release (Protonix Delayed-Release) by Wyeth/Pfizer for the treatment o…
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FDA approval · 2007-10-22FDA Approved: OMEPRAZOLE — Original Application (Apotex Corp)
FDA approved Apotex Corp's original application for a generic omeprazole product, enabling a generic option for treating gastroesophageal re…
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FDA approval · 2007-10-22FDA Approved: OMEPRAZOLE — Original Application (Quallent Pharmaceuticals Health LLC)
FDA approved the original (ANDA) application for omeprazole from Quallent Pharmaceuticals Health LLC, authorizing a generic omeprazole produ…
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FDA approval · 2007-09-21FDA Approved: RANITIDINE — Original Application (Pharmaceutical Associates, Inc.)
FDA approved an original application for ranitidine (generic) by Pharmaceutical Associates, Inc.
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FDA approval · 2007-08-31FDA Approved: RANITIDINE — Original Application (Dr. Reddy's Laboratories Limited)
FDA approved the original ANDA for ranitidine from Dr. Reddy's Laboratories Limited, enabling a generic ranitidine product to be marketed in…