Duodenal Ulcer
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Sign up freeTop drugs studied for this disease
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FDA approval · 2023-07-18FDA Approved: PROTONIX DELAYED-RELEASE — Supplemental Application (Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.)
The FDA approved a supplemental application for Protonix Delayed-Release (pantoprazole sodium) from Wyeth Pharmaceuticals (Pfizer). This act…
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FDA approval · 2023-07-18FDA Approved: ACIPHEX — Supplemental Application (Waylis Therapeutics LLC)
FDA approved a supplemental application for ACIPHEX (rabeprazole sodium) submitted by Waylis Therapeutics LLC.
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FDA approval · 2023-07-18FDA Approved: OMEPRAZOLE — Supplemental Application (Glenmark Pharmaceuticals Inc., USA)
FDA approved Glenmark's supplemental application for omeprazole (generic), granting changes to the approved ANDA product labeling.
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FDA approval · 2023-07-18FDA Approved: LANSOPRAZOLE, AMOXICILLIN, CLARITHROMYCIN — Supplemental Application (Rising Pharma Holdings, Inc.)
The FDA granted supplemental approval for a lansoprazole-amoxicillin-clarithromycin combination product by Rising Pharma Holdings, Inc. to e…
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FDA approval · 2023-07-18FDA Approved: PANTOPRAZOLE SODIUM — Supplemental Application (Civica, Inc.)
FDA approved a supplemental application for pantoprazole sodium by Civica, Inc., likely involving labeling or indication changes.
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FDA approval · 2023-07-18FDA Approved: OMEPRAZOLE AND SODIUM BICARBONATE — Supplemental Application (Oceanside Pharmaceuticals)
The FDA approved Oceanside Pharmaceuticals' supplemental application for omeprazole and sodium bicarbonate, updating the product labeling ac…
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FDA approval · 2023-07-18FDA Approved: OMEPRAZOLE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for omeprazole by Aurobindo Pharma Limited. The action provides regulatory clearance for the generic…
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FDA approval · 2023-07-18FDA Approved: OMEPRAZOLE — Supplemental Application (Golden State Medical Supply, Inc.)
FDA approved a supplemental application for the generic drug omeprazole from Golden State Medical Supply, Inc.
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FDA approval · 2023-07-12FDA Approved: ESOMEPRAZOLE MAGNESIUM — Original Application (Aurohealth LLC)
FDA approved esomeprazole magnesium as a generic drug from Aurohealth LLC under ANDA 214473.
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FDA approval · 2023-07-07FDA Approved: FAMOTIDINE — Original Application (Biocon Pharma Inc.)
FDA approved Biocon Pharma Inc.'s original ANDA for famotidine, enabling a generic version of the H2 blocker for the treatment and preventio…
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FDA approval · 2023-06-30FDA Approved: LANSOPRAZOLE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approved a supplemental application for lansoprazole from Teva Pharmaceuticals USA, Inc., updating/expanding the approval for the generi…
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FDA approval · 2023-06-16FDA Approved: FAMOTIDINE — Original Application (Upsher-Smith Laboratories, LLC)
FDA approves the original Abbreviated New Drug Application for famotidine from Upsher-Smith Laboratories, LLC, granting a generic version of…
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FDA approval · 2023-06-07FDA Approved: ESOMEPRAZOLE MAGNESIUM — Original Application (Zydus Pharmaceuticals USA Inc.)
FDA approved the original application for esomeprazole magnesium (generic) from Zydus Pharmaceuticals USA Inc. The approval covers the same …
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FDA approval · 2023-05-22FDA Approved: ESOMEPRAZOLE MAGNESIUM — Supplemental Application (Sun Pharmaceutical Industries, Inc)
FDA approved Sun Pharmaceutical Industries' supplemental application for esomeprazole magnesium (generic), a proton pump inhibitor, under th…
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FDA approval · 2023-05-22FDA Approved: ESOMEPRAZOLE MAGNESIUM — Supplemental Application (Ascend Laboratories, LLC)
The FDA approved Ascend Laboratories' supplemental application for esomeprazole magnesium delayed-release capsules (generic esomeprazole mag…
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FDA approval · 2023-04-28FDA Approved: OMEPRAZOLE — Original Application (Aurohealth LLC)
FDA approved Aurohealth LLC's original ANDA for omeprazole, enabling the marketing of a generic proton pump inhibitor in the United States. …
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FDA approval · 2023-04-27FDA Approved: ESOMEPRAZOLE MAGNESIUM — Supplemental Application (Camber Pharmaceuticals, Inc.)
The FDA approved Camber Pharmaceuticals' supplemental application for Esomeprazole Magnesium, a generic proton pump inhibitor, marking a rou…
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FDA approval · 2023-04-06FDA Approved: PANTOPRAZOLE SODIUM — Supplemental Application (Mylan Pharmaceuticals Inc.)
The FDA approved a supplemental application for pantoprazole sodium from Mylan Pharmaceuticals Inc., granting approval of a generic pantopra…
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FDA approval · 2023-03-30FDA Approved: RABEPRAZOLE SODIUM — Supplemental Application (Advagen Pharma Limited)
FDA approved a supplemental application for rabeprazole sodium filed by Advagen Pharma Limited, indicating an approved amendment to an exist…
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FDA approval · 2023-03-28FDA Approved: ESOMEPRAZOLE MAGNESIUM — Original Application (Solco Healthcare US LLC)
FDA approves esomeprazole magnesium under an Original Application for Solco Healthcare US LLC, enabling a generic version of the proton pump…
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FDA approval · 2023-03-08FDA Approved: ESOMEPRAZOLE SODIUM — Supplemental Application (Gland Pharma Limited)
FDA approved a supplemental application for esomeprazole sodium from Gland Pharma Limited, expanding the generic's regulatory approval. The …
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FDA approval · 2023-02-09FDA Approved: PANTOPRAZOLE SODIUM — Original Application (Ajanta Pharma USA Inc.)
FDA approved Pantoprazole Sodium as an original generic product (ANDA 217416) for Ajanta Pharma USA Inc., expanding access to pantoprazole s…
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FDA approval · 2022-11-01FDA Approved: EQUATE LANSOPRAZOLE — Supplemental Application (Wal-Mart Stores Inc)
FDA approved a supplemental application for Equate Lansoprazole, Wal-Mart's store-brand lansoprazole. The approval confirms the Wal-Mart Sto…
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FDA approval · 2022-09-30FDA Approved: GOOD NEIGHBOR PHARMACY OMEPRAZOLE — Supplemental Application (Amerisource Bergen)
FDA granted a supplemental approval for Good Neighbor Pharmacy Omeprazole (omeprazole) from AmerisourceBergen.
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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.