Vomiting
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Sign up freeTop drugs studied for this disease
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EMA approval · 2026-08-25EMA Authorised: Akynzeo (netupitant;palonosetron hydrochloride) — Helsinn Birex Pharmaceuticals Ltd
The EMA authorised Akynzeo (netupitant and palonosetron hydrochloride) for vomiting, nausea, cancer-related indications.
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FDA approval · 2026-04-01FDA Approved: PROCHLORPERAZINE EDISYLATE — Supplemental Application (Somerset Therapeutics, LLC)
FDA approved a supplemental application for PROCHLORPERAZINE EDISYLATE (ANDA212257) filed by Somerset Therapeutics, LLC. This approval relat…
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FDA approval · 2025-09-08FDA Approved: PROCHLORPERAZINE MALEATE — Original Application (Aurobindo Pharma Limited)
The FDA approved Aurobindo Pharma Limited's original ANDA for prochlorperazine maleate, allowing the generic antiemetic/antipsychotic to be …
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FDA approval · 2025-06-24FDA Approved: PROMETHAZINE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for promethazine hydrochloride from Hikma Pharmaceuticals USA, confirming the approval of a generic …
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FDA approval · 2025-01-22FDA Approved: PROCHLORPERAZINE MALEATE — Supplemental Application (Ajanta Pharma USA Inc.)
FDA approved a supplemental application for PROCHLORPERAZINE MALEATE by Ajanta Pharma USA Inc. under the ANDA pathway.
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FDA approval · 2024-09-13FDA Approved: PROCHLORPERAZINE EDISYLATE — Original Application (Somerset Therapeutics, LLC)
FDA approved the original ANDA for Prochlorperazine Edisylate from Somerset Therapeutics, LLC, authorizing its marketing as an antiemetic fo…
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FDA approval · 2023-05-01FDA Approved: ONDANSETRON HYDROCHLORIDE — Supplemental Application (Onesource Specialty Pharma Limited)
The FDA approved a supplemental application for ondansetron hydrochloride from Onesource Specialty Pharma Limited, approving this generic an…
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FDA approval · 2023-04-04FDA Approved: PROCHLORPERAZINE MALEATE — Original Application (Bionpharma Inc.)
FDA approved an Original Application for Prochlorperazine Maleate from Bionpharma Inc., authorizing its marketing as a generic antiemetic.
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FDA approval · 2023-03-17FDA Approved: PROCHLORPERAZINE MALEATE — Original Application (GLENMARK PHARMACEUTICALS INC., USA)
FDA approved Prochlorperazine maleate from Glenmark Pharmaceuticals under an Original Application; it is an antiemetic indicated to prevent …
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EMA approval · 2023-02-24EMA Authorised: Aloxi (palonosetron hydrochloride) — Helsinn Birex Pharmaceuticals Ltd.
Aloxi (palonosetron hydrochloride) has been authorised in the EU for use related to vomiting and cancer indications.
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FDA approval · 2022-07-14FDA Approved: PROCHLORPERAZINE EDISYLATE — Original Application (Eugia US LLC)
FDA approves the original application for Prochlorperazine edisylate (generic) by Eugia US LLC.
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FDA approval · 2022-03-15FDA Approved: ONDANSETRON — Supplemental Application (Hospira, Inc.)
FDA approves Hospira, Inc.'s supplemental application for ondansetron, authorizing changes to the approved product.
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FDA approval · 2021-09-28FDA Approved: PROCHLORPERAZINE EDISYLATE — Original Application (Cosette Pharmaceuticals, Inc.)
FDA approves Cosette Pharmaceuticals' prochlorperazine edisylate as an original generic application for use as an antiemetic.
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FDA approval · 2021-07-12FDA Approved: PROMETHAZINE HYDROCHLORIDE — Original Application (QUAGEN PHARMACEUTICALS LLC)
FDA approved promethazine hydrochloride under an original ANDA for Quagen Pharmaceuticals LLC.
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FDA approval · 2021-04-22FDA Approved: PROCHLORPERAZINE EDISYLATE — Original Application (Caplin Steriles Limited)
FDA approved the original application for PROCHLORPERAZINE EDISYLATE (Caplin Steriles Limited), a prochlorperazine edisylate antiemetic prod…
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FDA approval · 2020-06-25FDA Approved: PROCHLORPERAZINE EDISYLATE — Supplemental Application (Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)
FDA approved a supplemental application for Prochlorperazine Edisylate from Heritage Pharmaceuticals (d/b/a Avet Pharmaceuticals).
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FDA approval · 2018-10-25FDA Approved: PROCHLORPERAZINE EDISYLATE — Original Application (Mylan Institutional LLC)
The FDA approved the original ANDA for Prochlorperazine Edisylate by Mylan Institutional LLC, enabling a generic version of this antiemetic.…
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FDA approval · 2017-03-24FDA Approved: ONDANSETRON HYDROCHLORIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for ondansetron hydrochloride from Sun Pharmaceutical Industries, Inc., under the ANDA.
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FDA approval · 2017-02-23FDA Approved: PROCHLORPERAZINE — Supplemental Application (Cosette Pharmaceuticals, Inc.)
FDA approved a supplemental application for prochlorperazine submitted by Cosette Pharmaceuticals, Inc. under ANDA 040058.
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FDA approval · 2017-02-23FDA Approved: CHLORPROMAZINE HYDROCHLORIDE — Supplemental Application (Upsher-Smith Laboratories, LLC)
The FDA approved a supplemental application for chlorpromazine hydrochloride (Upsher-Smith Laboratories), updating an existing product's lab…
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FDA approval · 2015-10-26FDA Approved: ONDANSETRON HYDROCHLORIDE — Supplemental Application (Onesource Specialty Pharma Limited)
FDA approved a supplemental application for ondansetron hydrochloride from Onesource Specialty Pharma Limited. This action updates the regul…
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FDA approval · 2015-04-03FDA Approved: ONDANSETRON — Supplemental Application (Qilu Pharmaceutical Co., Ltd.)
FDA approved a supplemental application for ondansetron from Qilu Pharmaceutical Co., Ltd. (ANDA 203711), authorizing a supplemental submiss…
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FDA approval · 2013-10-15FDA Approved: PROCHLORPERAZINE EDISYLATE — Original Application (Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)
FDA approved the original application for Prochlorperazine edisylate, a generic product, manufactured by Heritage Pharmaceuticals Inc. (d/b/…
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FDA approval · 2013-08-30FDA Approved: ONDANSETRON HYDROCHLORIDE — Supplemental Application (Onesource Specialty Pharma Limited)
FDA approved a supplemental application for ondansetron hydrochloride from Onesource Specialty Pharma Limited to permit the marketing of thi…
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FDA approval · 2012-06-28FDA Approved: PROMETHAZINE HYDROCHLORIDE — Original Application (Cranbury Pharmaceuticals, LLC)
The FDA approved Promethazine hydrochloride as an original generic drug application (ANDA) for Cranbury Pharmaceuticals, LLC.