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You are here: Industry Insights > onabotulinumtoxinA

News List

FDA Approves Expanded Botox (onabotulinumtoxinA) Label to Include Eight New Muscles to Treat Adults with Upper Limb Spasticity drugs
August 02, 2021
Allergan, an AbbVie (NYSE: ABBV) company, today announced that the U.S. Food and Drug Administration (FDA) has approved a label expansion of Botox® to include eight new muscles for the treatment of upper limb spasticity in adults.
FDA Approves Botox (onabotulinumtoxinA) for Pediatric Patients with Upper Limb Spasticity drugs
June 24, 2019
FDA Approves Botox (onabotulinumtoxinA) for Pediatric Patients with Upper Limb Spasticity.

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