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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 | Illinois

PRINCETON, N.J. & DEERFIELD, Ill. (BUSINESS WIRE) May 10, 2023 ....

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FDA Approves Otsuka and Lundbeck's ABILIFY ASIMTUFII® (aripiprazole), the First Once-Every-Two-Months Long-acting Injectable (LAI) for the Treatment of Schizophrenia or Maintenance Monotherapy Treatment of Bipolar I Disorder in Adults | Illinois

PRINCETON, N.J. & DEERFIELD, Ill. (BUSINESS WIRE) Apr 27, 2023 ....

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Otsuka and Lundbeck Issue Statement on U.S. Food and Drug Administration (FDA) Advisory Committee Meeting on REXULTI® (brexpiprazole) for the Treatment of Agitation Associated with Alzheimer's Dementia | Illinois

PRINCETON, N.J. & DEERFIELD, Ill. (BUSINESS WIRE) Apr 16, 2023 ....

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