Duodenal Ulcer
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Sign up freeTop drugs studied for this disease
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FDA approval · 2015-08-27FDA Approved: SUCRALFATE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved a supplemental application for sucralfate from Teva Pharmaceuticals USA, Inc., indicating approval of a change to an existi…
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FDA approval · 2015-08-19FDA Approved: OMEPRAZOLE — Original Application (Aurobindo Pharma Limited)
The FDA approved Aurobindo Pharma Limited's original application for a generic omeprazole product.
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FDA approval · 2015-07-31FDA Approved: RABEPRAZOLE SODIUM — Original Application (Amneal Pharmaceuticals LLC)
FDA approved the Original Application for a generic rabeprazole sodium product by Amneal Pharmaceuticals. The approval supporting use for ac…
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CLINICAL_TRIALS trial_result · 2015-06-25Clinical Trial Update: Long-term Use of Takepron Capsules on the Prevention of Recurrence of Gastric/Duodenal Ulcer in Patients Receiving Low-dose Aspirin
A completed Takeda trial evaluating long-term use of Takepron capsules to prevent recurrence of gastric and duodenal ulcers in patients taki…
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CLINICAL_TRIALS trial_result · 2015-06-11Clinical Trial Update: MK0782 + Low-Dose Aspirin 7-Day Erosion Endoscopy Study (0782-001) [Phase 2]
A Phase 2 trial (0782-001) evaluating MK0782 with low-dose aspirin for a 7-day erosion endoscopy in gastric and duodenal ulcers has complete…
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FDA approval · 2015-06-01FDA Approved: GOOD NEIGHBOR PHARMACY OMEPRAZOLE — Supplemental Application (Amerisource Bergen)
The FDA approved a supplemental application for Good Neighbor Pharmacy Omeprazole (omeprazole) submitted by AmerisourceBergen, allowing the …
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FDA approval · 2015-05-06FDA Approved: PEPCID AC MAXIMUM STRENGTH — Supplemental Application (Kenvue Brands LLC)
FDA approved a supplemental application for Pepcid AC Maximum Strength (famotidine) submitted by Kenvue Brands LLC. This action expands the …
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FDA approval · 2015-04-20FDA Approved: PEPCID AC MAXIMUM STRENGTH — Supplemental Application (Kenvue Brands LLC)
FDA approved a supplemental application for Pepcid AC Maximum Strength (famotidine) filed by Kenvue Brands LLC to update the OTC product lab…
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FDA approval · 2015-04-14FDA Approved: OMEPRAZOLE — Supplemental Application (Sandoz Inc)
The FDA approved Sandoz Inc's supplemental application for omeprazole, a generic proton pump inhibitor.
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FDA approval · 2015-04-09FDA Approved: PANTOPRAZOLE SODIUM — Supplemental Application (Torrent Pharmaceuticals Limited)
FDA approved a supplemental application for Pantoprazole Sodium from Torrent Pharmaceuticals Limited under the ANDA program. This action upd…
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FDA approval · 2015-04-08FDA Approved: PANTOPRAZOLE — Supplemental Application (NorthStar RxLLC)
FDA approves a supplemental application for pantoprazole from NorthStar RxLLC, indicating approval of a generic pantoprazole product.
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FDA approval · 2015-04-08FDA Approved: PANTOPRAZOLE SODIUM — Supplemental Application (NorthStar Rx LLC)
FDA approved a supplemental application for Pantoprazole Sodium from NorthStar Rx LLC under an ANDA (202038), authorizing regulatory action …
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FDA approval · 2015-04-03FDA Approved: RABEPRAZOLE SODIUM — Supplemental Application (Lannett Company, Inc.)
FDA approved a supplemental application for Lannett's generic rabeprazole sodium (ANDA 090678), authorizing its marketing as a proton pump i…
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FDA approval · 2015-04-02FDA Approved: RABEPRAZOLE SODIUM — Supplemental Application (Torrent Pharmaceuticals Limited)
The FDA approved a supplemental application for rabeprazole sodium from Torrent Pharmaceuticals Limited under ANDA 202376, indicating a post…
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FDA approval · 2015-03-20FDA Approved: OMEPRAZOLE — Supplemental Application (Apotex Corp)
FDA approved a supplemental application for omeprazole from Apotex Corp., authorizing a generic version of the drug.
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FDA approval · 2015-03-16FDA Approved: OMEPRAZOLE — Supplemental Application (Dr. Reddy's Laboratories Limited)
FDA approved a supplemental application for omeprazole submitted by Dr. Reddy's Laboratories Limited.
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FDA label_change · 2015-03-16FDA Approved: LANSOPRAZOLE — Supplemental Application (Mylan Pharmaceuticals Inc.)
FDA approved a supplemental application for lansoprazole submitted by Mylan Pharmaceuticals, indicating a change to the product labeling/aut…
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FDA approval · 2015-03-06FDA Approved: GOOD NEIGHBOR PHARMACY OMEPRAZOLE — Supplemental Application (Amerisource Bergen)
FDA approved a supplemental application for Good Neighbor Pharmacy Omeprazole (omeprazole) submitted by AmerisourceBergen, under NDA 022032.
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FDA approval · 2015-03-02FDA Approved: OMEPRAZOLE — Supplemental Application (Zydus Lifesciences Limited)
FDA approved a supplemental application for omeprazole from Zydus Lifesciences Limited under the ANDA.
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FDA approval · 2015-02-25FDA Approved: PANTOPRAZOLE SODIUM — Supplemental Application (Torrent Pharmaceuticals Limited)
FDA has approved a supplemental application for Pantoprazole Sodium from Torrent Pharmaceuticals Limited, resulting in the approval of the g…
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FDA approval · 2015-01-02FDA Approved: PANTOPRAZOLE SODIUM — Supplemental Application (NorthStar Rx LLC)
The FDA approved a supplemental application for pantoprazole sodium filed by NorthStar Rx LLC.
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FDA approval · 2015-01-02FDA Approved: OMEPRAZOLE — Supplemental Application (Quallent Pharmaceuticals Health LLC)
FDA approves a supplemental application for omeprazole from Quallent Pharmaceuticals Health LLC, authorizing an additional formulation/produ…
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FDA approval · 2014-12-21FDA Approved: PANTOPRAZOLE — Supplemental Application (NorthStar RxLLC)
The FDA approved a supplemental application for pantoprazole submitted by NorthStar RxLLC under the ANDA pathway.
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FDA approval · 2014-12-19FDA Approved: NEXIUM — Supplemental Application (AstraZeneca Pharmaceuticals LP)
FDA approved a supplemental application for Nexium (esomeprazole magnesium) submitted by AstraZeneca Pharmaceuticals LP.
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FDA approval · 2014-12-19FDA Approved: PREVACID SOLUTAB — Supplemental Application (Takeda Pharmaceuticals America, Inc.)
The FDA approved a supplemental application for PREVACID SOLUTAB (lansoprazole) by Takeda Pharmaceuticals America, Inc.