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Daxxify, a New Anti-Wrinkle Drug and Botox Competitor is FDA-Approved

XTalks

Daxxify was FDA-approved for similar cosmetic purposes as Botox and other neuromodulators like Dysport and Xeomin. One of the first options made available for such purposes was Botox from Allergan, brought to health practitioners’ offices in 1989. A Novel Botox Competitor.

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Letybo Earns FDA Approval, Hugel Expands Its Global Aesthetic Market Leadership

XTalks

Among the most widely sought-after options are botulinum toxin injections, commonly referred to as Botox or Dysport. RELATED: Innovations and Clinical Trial Diversity in Medical Aesthetics: Insights from Dr. Stephanie Manson Brown, VP & Head of Clinical Development at Allergan Aesthetics – Xtalks Life Science Podcast Ep.

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Top 20 Best-Selling Neurology Drugs to Watch in 2024

XTalks

Price of Botox: Cost depends heavily on the condition and dose required, but the list price is $1,292 for a 200-unit vial. Why it sold so well: Botox is FDA-approved for the treatment of chronic migraines and that is currently the only chronic condition for which it has received approval. billion in the US and $4.1

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Top 30 Drugs to Watch in 2024: Insights from 2023 Sales Data

XTalks

Keytruda (Pembrolizumab) Keytruda 2023 Sales: $25.011 billion Company/Developer: Merck Date of First US Food and Drug Administration (FDA) Approval: September 4, 2014 Indications Keytruda Is FDA-Approved for: Unresectable or metastatic melanoma.

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AbbVie Reports Second-Quarter 2021 Financial Results

The Pharma Data

Global Botox Therapeutic net revenues were $603 million, an increase of over 100.0 Global Botox Cosmetic net revenues were $584 million, an increase of over 100.0 AbbVie also presented real-world data on the role of Botox in combination with CGRP mAbs for Chronic Migraine prevention. percent on a reported basis, or 29.6

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Top 30 Pharma and Biotech Companies in 2023: Statistics and Trends

XTalks

Paxlovid was first authorized under the FDA Emergency Use Authorization in December 2021 ; however, it has received FDA approval on May 25, 2023. pneumoniae serotypes) replaced the company’s first pneumococcal conjugate vaccine Prevnar (PCV7, approved by the FDA in February 2000) in a February 2010 FDA approval.

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