Centanafadine is an Otsuka Pharmaceutical program in ADHD in adults and pediatric patients aged 6 years and older (≥20kg). The FDA approved it on Jul 24, 2026. 1 FDA decision on record below. Every date links its source.
All upcoming FDA decision dates on the 2026 PDUFA calendar
FDA approval tracked on pdufa.bio: ADHD in adults and pediatric patients aged 6 years and older (≥20kg) (approved Jul 24, 2026). Earlier approvals may not be listed here; the FDA label is the full record. Sponsor: Otsuka Pharmaceutical (OTSKY). Market-cap tier at the time we tracked it: Large. We track 1 catalyst event for this program: 0 upcoming and 1 in the record. A PDUFA date is the FDA's target date to complete review of a marketing application; a readout is the sponsor's expected date for clinical trial results. What a PDUFA date is · why we do not compare trial results across drugs.
No upcoming catalyst is on our calendar for Centanafadine; 1 FDA decision is on record below.
On Jul 24, 2026 the FDA approved the application. The decision page carries the source document and the measured share-price reaction.
In our records Centanafadine is FDA-approved for ADHD in adults and pediatric patients aged 6 years and older (≥20kg) (approved Jul 24, 2026). Other approved uses may not be tracked here; the FDA label is the full record.
Otsuka Pharmaceutical (OTSKY).
Yes. The FDA approved an application for Centanafadine on Jul 24, 2026; the decision page linked above carries the source.
FDA announcements, sponsor press releases and SEC filings; every date on this page links its source.