Von Willebrand Disease
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Sign up freeTop drugs studied for this disease
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EMA approval · 2026-07-15EMA Authorised: Veyvondi (vonicog alfa) — Baxalta Innovations GmbH
EMA authorised Veyvondi (vonicog alfa) by Baxalta Innovations GmbH for von Willebrand diseases.
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FDA approval · 2026-02-27FDA Approved: DESMOPRESSIN ACETATE — Original Application (Caplin Steriles Limited)
FDA approved Desmopressin Acetate from Caplin Steriles Limited under an Original Application (ANDA). This marks the approval of a generic De…
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FDA approval · 2026-02-25FDA Approved: DESMODA — Original Application (Eton Pharmaceuticals, Inc.)
FDA approves DESMODA (desmopressin acetate oral solution) under an original NDA from Eton Pharmaceuticals; the product provides a new oral f…
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EMA approval · 2026-01-20EMA Authorised: Veyvondi (vonicog alfa) — Baxalta Innovations GmbH
The European Medicines Agency authorised Veyvondi (vonicog alfa) by Baxalta Innovations GmbH for the treatment of von Willebrand disease. Th…
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FDA approval · 2025-08-27FDA Approved: DESMOPRESSIN ACETATE — Supplemental Application (Avenacy, Inc.)
FDA approved a supplemental application for Desmopressin Acetate by Avenacy, Inc.
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EMA approval · 2024-12-18EMA Authorised: Voncento (human coagulation factor VIII;human von willebrand factor) — CSL Behring GmbH
The EMA authorised Voncento, a Factor VIII/von Willebrand factor concentrate by CSL Behring, for treatment of Hemophilia A and von Willebran…
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FDA approval · 2024-03-21FDA Approved: DESMOPRESSIN ACETATE — Original Application (Aurobindo Pharma Limited)
FDA approved desmopressin acetate from Aurobindo Pharma Limited under an original abbreviated new drug application (ANDA213095).
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FDA approval · 2022-11-16FDA Approved: DESMOPRESSIN ACETATE — Original Application (Fresenius Kabi USA, LLC)
FDA approved the Original Application for Desmopressin Acetate from Fresenius Kabi USA, LLC (ANDA216922). This marks the approval of a gener…
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FDA approval · 2022-08-19FDA Approved: DESMOPRESSIN ACETATE — Original Application (Dr. Reddy's Laboratories Inc.)
FDA approved Desmopressin Acetate from Dr. Reddy's Laboratories Inc. via an Original Application for a generic product.
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FDA approval · 2019-10-24FDA Approved: DESMOPRESSIN ACETATE — Supplemental Application (Apotex Corp.)
FDA approves Apotex Corp.'s supplemental application for Desmopressin Acetate, enabling the generic version to be marketed.
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FDA approval · 2019-01-28FDA Approved: DESMOPRESSIN ACETATE — Original Application (KVK-TECH, INC.)
The FDA approved Desmopressin Acetate from KVK-Tech under an Original Application, providing a new generic option for this drug product.
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FDA approval · 2017-08-22FDA Approved: DESMOPRESSIN ACETATE — Original Application (Sagent Pharmaceuticals)
FDA approved the Original Application for Desmopressin Acetate (DESMOPRESSIN ACETATE) by Sagent Pharmaceuticals, providing a generic version…
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FDA approval · 2017-08-22FDA Approved: DESMOPRESSIN ACETATE — Original Application (Sagent Pharmaceuticals)
FDA approved an original application for Desmopressin Acetate from Sagent Pharmaceuticals, establishing a generic version of the product.
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FDA approval · 2017-05-26FDA Approved: DESMOPRESSIN ACETATE — Original Application (Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)
FDA approved an Original Application for Desmopressin Acetate as a generic product manufactured by Heritage Pharmaceuticals Inc. d/b/a Avet …
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FDA approval · 2015-05-28FDA Approved: DESMOPRESSIN ACETATE — Original Application (Glenmark Pharmaceuticals Inc.,USA)
The FDA approved Glenmark's Desmopressin Acetate as an Original Application (ANDA201831), authorizing the generic product to be marketed for…
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FDA approval · 2015-01-23FDA Approved: DESMOPRESSIN ACETATE — Supplemental Application (Apotex Corp.)
FDA approved a supplemental application for Desmopressin Acetate from Apotex Corp. under an ANDA.
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FDA approval · 2015-01-14FDA Approved: DESMOPRESSIN ACETATE — Supplemental Application (Bauch & Lomb Incorporated)
FDA approved a supplemental application for desmopressin acetate from Bauch & Lomb Incorporated under an ANDA.
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FDA approval · 2014-02-28FDA Approved: DDAVP — Supplemental Application (Ferring Pharmaceuticals Inc.)
The FDA approved a supplemental application for DDAVP (desmopressin acetate) filed by Ferring Pharmaceuticals Inc. The action updates the pr…
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FDA approval · 2013-01-25FDA Approved: DESMOPRESSIN ACETATE — Original Application (Sun Pharmaceutical Industries, Inc.)
FDA approved an Abbreviated New Drug Application for Desmopressin Acetate from Sun Pharmaceutical Industries, marking a generic product appr…
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FDA approval · 2009-03-27FDA Approved: DESMOPRESSIN ACETATE — Supplemental Application (Meitheal Pharmaceuticals Inc.)
FDA approved a supplemental application for Desmopressin Acetate submitted by Meitheal Pharmaceuticals Inc.
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FDA approval · 2008-09-03FDA Approved: DESMOPRESSIN ACETATE — Supplemental Application (Apotex Corp.)
FDA approved a supplemental application for Desmopressin Acetate from Apotex Corp., indicating an addition or modification to the approved p…
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FDA approval · 2008-03-11FDA Approved: DESMOPRESSIN ACETATE — Supplemental Application (Apotex Corp.)
FDA approved a supplemental application for Desmopressin Acetate from Apotex Corp., updating the approved generic product. The action formal…
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FDA approval · 2007-10-26FDA Approved: DDAVP — Supplemental Application (Ferring Pharmaceuticals Inc.)
FDA approved a supplemental application for DDAVP (desmopressin acetate) from Ferring Pharmaceuticals Inc., updating the product's labeling.
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FDA approval · 2007-05-23FDA Approved: DESMOPRESSIN ACETATE — Supplemental Application (Apotex Corp.)
FDA approved a supplemental application for Desmopressin Acetate submitted by Apotex Corp. under an ANDA.
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FDA approval · 2006-12-03FDA Approved: DESMOPRESSIN ACETATE — Supplemental Application (Apotex Corp.)
FDA granted a supplemental approval for Desmopressin Acetate from Apotex Corp. under an ANDA, authorizing its generic product.