Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA) Approval of Supplemental New Drug Application (sNDA) for REXULTI® (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due to Alzheimer's Disease

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Last updated 03 janeiro 2025
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
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Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
News Releases Otsuka Pharmaceutical Co., Ltd.
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
FDA - Denmark
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Piyush Dham on LinkedIn: The caring company: At Otsuka America
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Dementia - Drug Discovery World (DDW)
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Mischa Agster on LinkedIn: Otsuka Announces New FDA Approval
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Clinical Catch-Up: Alzheimer's, MS and Cancer Headline Trial News
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Allison Rosenthal on LinkedIn: InTOW Accepting Applications for
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
H. Lundbeck A/S and Otsuka Pharmaceutical, Co. Ltd. Announce U.S.
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Otsuka and Lundbeck Announce U.S. Food and Drug Administration
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Allison Rosenthal on LinkedIn: #worldmentalhealthday
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Allison Rosenthal على LinkedIn: National Family Caregivers Month
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Otsuka, Lundbeck's sNDA for Rexulti received US FDA approval
Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA)  Approval of Supplemental New Drug Application (sNDA) for REXULTI®  (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due  to Alzheimer's Disease
Dementia - Drug Discovery World (DDW)

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