Important Update About the Discontinuation of Commercialization of ABILIFY MYCITE® 

In October 2024, Otsuka Pharmaceutical Co., and Otsuka America Pharmaceutical, Inc. elected to discontinue commercialization of the ABILIFY MYCITE® System (aripiprazole tablet with sensor) in the U.S.

Our immediate priority is to provide a seamless transition for patients and healthcare professionals during this time.

ABILIFY MYCITE®, the world’s first U.S. FDA-approved digital medicine, launched in 2017 and represents an important milestone in Otsuka’s commitment to introducing innovative treatment options to people living with chronic, serious mental illness.  We have gained valuable insights and key learnings and will continue to monitor healthcare trends and use our deep knowledge and experience to develop new solutions.   
If you have any questions, please contact (1-800-441-6763).

November 2024          12US24EBC0038

 

Our Products

Below is a full list of the products marketed and commercialized in the US by OAPI that have been either developed, acquired, or in-licensed by Otsuka. Our product specialties include neuroscience, digital innovation, nephrology, oncology, and medical devices.

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Neuroscience

ABILIFY ASIMTUFII®
(aripiprazole) for extended release injectable suspension

ABILIFY MAINTENA®
(aripiprazole) for
extended release
injectable suspension

NUEDEXTA®
(dextromethorphan HBr and quinidine sulfate) capsules

Digital Innovation

Oncology

To report an adverse event or
product quality complaint,
please call 1-800-438-9927

To discuss a medical
inquiry, call 1-800-441-6763