Erosive Esophagitis
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Sign up freeTop drugs studied for this disease
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FDA approval · 2022-09-14FDA Approved: RABEPRAZOLE SODIUM — Supplemental Application (Aurobindo Pharma Limited)
The FDA approved a supplemental application for Rabeprazole sodium submitted by Aurobindo Pharma Limited.
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FDA approval · 2022-09-14FDA Approved: RABEPRAZOLE SODIUM — Supplemental Application (Ascend Laboratories, LLC)
FDA approved a supplemental application for rabeprazole sodium (Ascend Laboratories, LLC). This indicates regulatory approval of the generic…
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FDA approval · 2022-08-29FDA Approved: PANTOPRAZOLE SODIUM — Original Application (Northstar Rx LLC)
FDA approved Pantoprazole sodium as an original ANDA for a generic product manufactured by Northstar Rx LLC.
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FDA approval · 2022-08-25FDA Approved: ZANTAC 360 — Supplemental Application (Chattem, Inc.)
The FDA approved a supplemental application for ZANTAC 360 (famotidine) submitted by Chattem, Inc., under ANDA206531.
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FDA approval · 2022-08-15FDA Approved: PANTOPRAZOLE — Supplemental Application (NorthStar RxLLC)
The FDA approved a supplemental application for pantoprazole filed by NorthStar RxLLC.
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FDA approval · 2022-08-11FDA Approved: PANTOPRAZOLE SODIUM — Supplemental Application (Torrent Pharmaceuticals Limited)
FDA approved a supplemental application for pantoprazole sodium from Torrent Pharmaceuticals Limited. The action is a supplemental approval,…
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FDA approval · 2022-08-04FDA Approved: FAMOTIDINE — Original Application (Amneal Pharmaceuticals NY LLC)
FDA approves Amneal's original application for famotidine, enabling a generic version of the H2 blocker. The approval covers common indicati…
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CLINICAL_TRIALS trial_result · 2022-07-29Clinical Trial Update: Efficacy and Safety of Vonoprazan Compared to Lansoprazole in Participants With Erosive Esophagitis [Phase 3]
Phase 3 trial comparing vonoprazan to lansoprazole in erosive esophagitis completed.
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FDA approval · 2022-07-28FDA Approved: PANTOPRAZOLE SODIUM — Supplemental Application (Eugia US LLC)
The FDA approved a supplemental application for pantoprazole sodium from Eugia US LLC. The action pertains to an already approved generic, t…
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FDA approval · 2022-07-26FDA Approved: PANTOPRAZOLE SODIUM DELAYED-RELEASE — Original Application (Lifestar Pharma LLC)
FDA approved pantoprazole sodium delayed-release through an original application for Lifestar Pharma LLC.
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CLINICAL_TRIALS trial_result · 2022-07-13Clinical Trial Update: Clinical Trial to Evaluate the Safety and Efficacy of JP-1366 in Patients With Erosive Gastroesophageal Reflux Disease [Phase 2]
Phase 2 clinical trial evaluating safety and efficacy of JP-1366 in patients with erosive gastroesophageal reflux disease (GERD) has complet…
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FDA approval · 2022-06-24FDA Approved: ESOMEPRAZOLE MAGNESIUM — Original Application (Rising Pharma Holdings, Inc.)
FDA approved the original ANDA for esomeprazole magnesium as a generic proton pump inhibitor manufactured by Rising Pharma Holdings, Inc.
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FDA approval · 2022-06-16FDA Approved: DEXLANSOPRAZOLE — Supplemental Application (ENDO USA, Inc.)
The FDA approved a supplemental application for dexlansoprazole submitted by ENDO USA, Inc.
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FDA approval · 2022-06-09FDA Approved: PANTOPRAZOLE SODIUM — Supplemental Application (Lannett Company, Inc.)
FDA approved a supplemental application for pantoprazole sodium from Lannett Company, enabling the marketing of this generic proton pump inh…
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FDA approval · 2022-06-09FDA Approved: PANTOPRAZOLE SODIUM — Supplemental Application (NorthStar Rx LLC)
FDA approved a supplemental application for pantoprazole sodium from NorthStar Rx LLC, a generic pantoprazole product.
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FDA approval · 2022-06-03FDA Approved: FAMOTIDINE — Original Application (Zydus Lifesciences Limited)
The FDA approved an original abbreviated new drug application (ANDA) for famotidine from Zydus Lifesciences Limited, making a generic versio…
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FDA approval · 2022-05-19FDA Approved: PANTOPRAZOLE SODIUM I.V. — Original Application (Piramal Critical Care)
FDA approved Pantoprazole sodium for injection (IV) from Piramal Critical Care under an original application.
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FDA approval · 2022-05-18FDA Approved: PANTOPRAZOLE SODIUM — Original Application (Novadoz Pharmaceuticals LLC)
The FDA approved Pantoprazole sodium from Novadoz Pharmaceuticals LLC under an Original Application (ANDA216171), adding a generic pantopraz…
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FDA approval · 2022-05-18FDA Approved: PANTOPRAZOLE SODIUM — Original Application (Camber Pharmaceuticals, Inc.)
FDA approves Camber Pharmaceuticals' pantoprazole sodium as an original ANDA generic product. It is indicated for GERD-related conditions su…
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FDA approval · 2022-05-03FDA Approved: DEXLANSOPRAZOLE — Supplemental Application (ENDO USA, Inc.)
The FDA approved a supplemental application for a generic Dexlansoprazole from ENDO USA, Inc., enabling market availability.
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FDA approval · 2022-03-04FDA Approved: ACIPHEX — Supplemental Application (Waylis Therapeutics LLC)
The FDA approved a supplemental application for ACIPHEX (rabeprazole sodium) by Waylis Therapeutics LLC. The snippet does not specify the ex…
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FDA approval · 2022-03-04FDA Approved: PREVACID SOLUTAB — Supplemental Application (Takeda Pharmaceuticals America, Inc.)
FDA approves a supplemental application for PREVACID SOLUTAB (lansoprazole) from Takeda Pharmaceuticals America, Inc.
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FDA approval · 2022-03-04FDA Approved: OMEPRAZOLE — Supplemental Application (Apotex Corp)
FDA approved a supplemental application for Omeprazole submitted by Apotex Corp.
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FDA approval · 2022-03-04FDA Approved: DEXILANT — Supplemental Application (Takeda Pharmaceuticals America, Inc.)
The FDA approved a supplemental application for Dexilant (dexlansoprazole) from Takeda Pharmaceuticals America, expanding or modifying its l…
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FDA approval · 2022-03-04FDA Approved: OMEPRAZOLE — Supplemental Application (Zydus Lifesciences Limited)
FDA approved a supplemental application for omeprazole submitted by Zydus Lifesciences Limited. The exact scope of the supplement (such as l…