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Hugel Received FDA Approval in the U.S. of Letybo (letibotulinumtoxinA-wlbg) for Injection for Treatment of Glabellar Lines
Biotechnology | FDA | Therapeutics

Hugel Received FDA Approval in the U.S. of Letybo (letibotulinumtoxinA-wlbg) for Injection for Treatment of Glabellar Lines

On Mar. 4, 2024, Hugel America announced it received U.S. Food and Drug Administration (FDA) approval on its…

Read More Hugel Received FDA Approval in the U.S. of Letybo (letibotulinumtoxinA-wlbg) for Injection for Treatment of Glabellar LinesContinue

U.S. FDA Approved First Therapeutic Indication for Revance’s DAXXIFY® (DaxibotulinumtoxinA-lanm) for the Treatment of Cervical Dystonia
Biotechnology | FDA | Therapeutics

U.S. FDA Approved First Therapeutic Indication for Revance’s DAXXIFY® (DaxibotulinumtoxinA-lanm) for the Treatment of Cervical Dystonia

On Apr. 14, 2023, Revance Therapeutics announced that the U.S. Food and Drug Administration (FDA) had approved the…

Read More U.S. FDA Approved First Therapeutic Indication for Revance’s DAXXIFY® (DaxibotulinumtoxinA-lanm) for the Treatment of Cervical DystoniaContinue

FDA Approved Daxxify, a New Anti-Wrinkle Drug
Biotechnology | FDA | Therapeutics

FDA Approved Daxxify, a New Anti-Wrinkle Drug

On Sept. 7, 2022, the U.S. Food and Drug Administration (FDA) announced it had approved Revance Therapeutics’ DAXXIFY…

Read More FDA Approved Daxxify, a New Anti-Wrinkle DrugContinue

FDA Approved Expanded BOTOX® Label to Include Eight New Muscles to Treat Adults with Upper Limb Spasticity
Biotechnology | FDA | Therapeutics

FDA Approved Expanded BOTOX® Label to Include Eight New Muscles to Treat Adults with Upper Limb Spasticity

On Jul. 29, 2021, BOTOX(R) Allergan, an AbbVie company, announced that the U.S. Food and Drug Administration (FDA)…

Read More FDA Approved Expanded BOTOX® Label to Include Eight New Muscles to Treat Adults with Upper Limb SpasticityContinue

BOTOX(R) cosmetic (onabotulinumtoxinA) approved by the FDA
Biotechnology | FDA | Therapeutics

BOTOX(R) cosmetic (onabotulinumtoxinA) approved by the FDA

On Apr. 15, 2002, BOTOX(R) cosmetic (onabotulinumtoxinA), manufactured by Allergan, was approved by the Food and Drug Administration…

Read More BOTOX(R) cosmetic (onabotulinumtoxinA) approved by the FDAContinue

BOTOX(R) cosmetic (onabotulinumtoxinA) approved by the FDA
Biotechnology | FDA | Therapeutics

BOTOX(R) cosmetic (onabotulinumtoxinA) approved by the FDA

On Dec. 29, 1989, the U.S. Food and Drug Administration (FDA) approved Oculinum’s (onabotulinumtoxinA) for treatment of strabismus…

Read More BOTOX(R) cosmetic (onabotulinumtoxinA) approved by the FDAContinue

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