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WELTRUZA

NDA · New Drug Application · Sponsor: TEVA NEUROSCIENCE INC · Approved 2026-10-08

Drug application

FDA Application #
NDA219007
Application type
New Drug Application
Brand name
WELTRUZA
Generic name
Olanzapine
Active ingredients
OLANZAPINE
Dosage form
SUSPENSION, EXTENDED RELEASE
Route
INJECTABLE
Marketing status
Prescription
Sponsor
TEVA NEUROSCIENCE INC
First approval
2026-10-08

Source

Authoritative
Drugs@FDA application overview
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